Canonical Allele Identifier: CA465127627
Gene: ALDH1B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.38396750T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.38396753T>C , CM000671.2:g.38396753T>C GRCh38
NC_000009.11:g.38396750T>C , CM000671.1:g.38396750T>C GRCh37
NC_000009.10:g.38386750T>C NCBI36
NG_012253.1:g.9049T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000377698.4:c.1005T>C MANE Select ENSP00000366927.3:p.Phe335=
ENST00000377698.3:c.1005T>C ENSP00000366927.3:p.Phe335=
NM_000692.4:c.1005T>C NP_000683.3:p.Phe335=
XM_011517802.1:c.1005T>C XP_011516104.1:p.Phe335=
XM_011517802.2:c.1005T>C XP_011516104.1:p.Phe335=
NM_000692.5:c.1005T>C MANE Select NP_000683.3:p.Phe335=
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