Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.45 (T)
Location

Chromosome 14:33241581 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 11 HGVS names - click the plus to show

14:g.33241581T>C
ENST00000549770.1:n.245+26155T>C
ENST00000551492.2:c.406+26155T>C
ENST00000548645.2:c.295+26155T>C
ENST00000357798.6:c.346+25994T>C
ENST00000546849.1:c.115+26155T>C
ENST00000356141.5:c.385+26155T>C
ENST00000551008.2:c.79+26155T>C
ENST00000547068.2:c.79+26155T>C
ENST00000551634.2:c.316+26155T>C
ENST00000346562.3:c.295+26155T>C

This variation has assays on 5 chips - click the plus to show

Variation displays