Canonical Allele Identifier: CA290433542

Gene: TCAP

Linked Data

• dbSNP Id: rs936447892
• gnomAD v3: 17-39665271-C-T
• gnomAD v4: 17-39665271-C-T
• MyVariant Identifiers: chr17:g.37821524C>T (hg19) ; chr17:g.39665271C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39665271C>T , CM000679.2:g.39665271C>T	GRCh38
NC_000017.10:g.37821524C>T , CM000679.1:g.37821524C>T	GRCh37
NC_000017.9:g.35075050C>T	NCBI36
NG_008892.1:g.4926C>T , LRG_210:g.4926C>T
NG_042278.1:g.2291C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.2:c.-89C>T	ENSP00000312624.2:n.-89C>T