Canonical Allele Identifier: CA8532808

Gene: TCAP

Linked Data

• dbSNP Id: rs756375255
• ExAC: 17:37821585 G / C
• gnomAD v2: 17-37821585-G-C
• MyVariant Identifiers: chr17:g.37821585G>C (hg19) ; chr17:g.39665332G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39665332G>C , CM000679.2:g.39665332G>C	GRCh38
NC_000017.10:g.37821585G>C , CM000679.1:g.37821585G>C	GRCh37
NC_000017.9:g.35075111G>C	NCBI36
NG_008892.1:g.4987G>C , LRG_210:g.4987G>C
NG_042278.1:g.2352G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000309889.2:c.-28G>C	ENSP00000312624.2:n.-28G>C