Canonical Allele Identifier: CA2617357411
Gene: TPI1 HGNC NCBI

Linked Data

gnomAD v4: 12-6867430-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6867430C>A , CM000674.2:g.6867430C>A GRCh38
NC_000012.11:g.6976594C>A , CM000674.1:g.6976594C>A GRCh37
NC_000012.10:g.6846855C>A NCBI36
NG_011948.1:g.5011C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000229270.8:c.-26C>A ENSP00000229270.4:n.-26C>A
ENST00000613953.4:c.-26C>A ENSP00000484435.1:n.-26C>A
NM_001159287.1:c.-26C>A NP_001152759.1:n.-26C>A
XR_002957378.1:n.597C>A
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