Canonical Allele Identifier: CA983629071
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs2057246379
gnomAD v3: 17-39665331-T-C
gnomAD v4: 17-39665331-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665331T>C , CM000679.2:g.39665331T>C GRCh38
NC_000017.10:g.37821584T>C , CM000679.1:g.37821584T>C GRCh37
NC_000017.9:g.35075110T>C NCBI36
NG_008892.1:g.4986T>C , LRG_210:g.4986T>C
NG_042278.1:g.2351T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000309889.2:c.-29T>C ENSP00000312624.2:n.-29T>C
Search 100 bp 5'
Search 100 bp 3'