Canonical Allele Identifier: CA290433586

Gene: TCAP

Linked Data

• dbSNP Id: rs768159521
• gnomAD v2: 17-37821556-G-T
• gnomAD v3: 17-39665303-G-T
• gnomAD v4: 17-39665303-G-T
• MyVariant Identifiers: chr17:g.37821556G>T (hg19) ; chr17:g.39665303G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39665303G>T , CM000679.2:g.39665303G>T	GRCh38
NC_000017.10:g.37821556G>T , CM000679.1:g.37821556G>T	GRCh37
NC_000017.9:g.35075082G>T	NCBI36
NG_008892.1:g.4958G>T , LRG_210:g.4958G>T
NG_042278.1:g.2323G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.2:c.-57G>T	ENSP00000312624.2:n.-57G>T