Canonical Allele Identifier: CA290433539

Gene: TCAP

Linked Data

• dbSNP Id: rs901021346
• gnomAD v3: 17-39665267-C-T
• gnomAD v4: 17-39665267-C-T
• MyVariant Identifiers: chr17:g.37821520C>T (hg19) ; chr17:g.39665267C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39665267C>T , CM000679.2:g.39665267C>T	GRCh38
NC_000017.10:g.37821520C>T , CM000679.1:g.37821520C>T	GRCh37
NC_000017.9:g.35075046C>T	NCBI36
NG_008892.1:g.4922C>T , LRG_210:g.4922C>T
NG_042278.1:g.2287C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.2:c.-93C>T	ENSP00000312624.2:n.-93C>T