Canonical Allele Identifier: CA465127458
Gene: ALDH1B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.38396666C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.38396669C>T , CM000671.2:g.38396669C>T GRCh38
NC_000009.11:g.38396666C>T , CM000671.1:g.38396666C>T GRCh37
NC_000009.10:g.38386666C>T NCBI36
NG_012253.1:g.8965C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000377698.4:c.921C>T MANE Select ENSP00000366927.3:p.Cys307=
ENST00000377698.3:c.921C>T ENSP00000366927.3:p.Cys307=
NM_000692.4:c.921C>T NP_000683.3:p.Cys307=
XM_011517802.1:c.921C>T XP_011516104.1:p.Cys307=
XM_011517802.2:c.921C>T XP_011516104.1:p.Cys307=
NM_000692.5:c.921C>T MANE Select NP_000683.3:p.Cys307=