Canonical Allele Identifier: CA2259200278
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs2057243494
gnomAD v4: 17-39664981-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39664981A>T , CM000679.2:g.39664981A>T GRCh38
NC_000017.10:g.37821234A>T , CM000679.1:g.37821234A>T GRCh37
NC_000017.9:g.35074760A>T NCBI36
NG_008892.1:g.4636A>T , LRG_210:g.4636A>T
NG_042278.1:g.2001A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-379A>T ENSP00000312624.2:n.-379A>T
Search 100 bp 5'
Search 100 bp 3'