Canonical Allele Identifier: CA625938788
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs1185139986

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665338G>A , CM000679.2:g.39665338G>A GRCh38
NC_000017.10:g.37821591G>A , CM000679.1:g.37821591G>A GRCh37
NC_000017.9:g.35075117G>A NCBI36
NG_008892.1:g.4993G>A , LRG_210:g.4993G>A
NG_042278.1:g.2358G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000309889.2:c.-22G>A ENSP00000312624.2:n.-22G>A