Canonical Allele Identifier: CA2593709979
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs2145070687
gnomAD v3: 17-39664931-C-G
gnomAD v4: 17-39664931-C-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39664931C>G , CM000679.2:g.39664931C>G GRCh38
NC_000017.10:g.37821184C>G , CM000679.1:g.37821184C>G GRCh37
NC_000017.9:g.35074710C>G NCBI36
NG_008892.1:g.4586C>G , LRG_210:g.4586C>G
NG_042278.1:g.1951C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-429C>G ENSP00000312624.2:n.-429C>G
Search 100 bp 5'
Search 100 bp 3'