Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K
Location

Chromosome 19:1401329 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM065210

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_064_GAMT_601240_0005, 10026

This variation has 5 HGVS names - click the plus to show

19:g.1401329T>G
ENST00000447102.5:c.148A>C
ENSP00000403536.2:p.Met50Leu
ENST00000252288.4:c.148A>C
ENSP00000252288.1:p.Met50Leu

Variation displays