Canonical Allele Identifier: CA465127562
Gene: ALDH1B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.38396714C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.38396717C>G , CM000671.2:g.38396717C>G GRCh38
NC_000009.11:g.38396714C>G , CM000671.1:g.38396714C>G GRCh37
NC_000009.10:g.38386714C>G NCBI36
NG_012253.1:g.9013C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000377698.4:c.969C>G MANE Select ENSP00000366927.3:p.Ser323=
ENST00000377698.3:c.969C>G ENSP00000366927.3:p.Ser323=
NM_000692.4:c.969C>G NP_000683.3:p.Ser323=
XM_011517802.1:c.969C>G XP_011516104.1:p.Ser323=
XM_011517802.2:c.969C>G XP_011516104.1:p.Ser323=
NM_000692.5:c.969C>G MANE Select NP_000683.3:p.Ser323=
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