Canonical Allele Identifier: CA465127589
Gene: ALDH1B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.38396726G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.38396729G>T , CM000671.2:g.38396729G>T GRCh38
NC_000009.11:g.38396726G>T , CM000671.1:g.38396726G>T GRCh37
NC_000009.10:g.38386726G>T NCBI36
NG_012253.1:g.9025G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000377698.4:c.981G>T MANE Select ENSP00000366927.3:p.Val327=
ENST00000377698.3:c.981G>T ENSP00000366927.3:p.Val327=
NM_000692.4:c.981G>T NP_000683.3:p.Val327=
XM_011517802.1:c.981G>T XP_011516104.1:p.Val327=
XM_011517802.2:c.981G>T XP_011516104.1:p.Val327=
NM_000692.5:c.981G>T MANE Select NP_000683.3:p.Val327=