Canonical Allele Identifier: CA2637631596
Gene: TCAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665087A>T , CM000679.2:g.39665087A>T GRCh38
NC_000017.10:g.37821340A>T , CM000679.1:g.37821340A>T GRCh37
NC_000017.9:g.35074866A>T NCBI36
NG_008892.1:g.4742A>T , LRG_210:g.4742A>T
NG_042278.1:g.2107A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-273A>T ENSP00000312624.2:n.-273A>T