Canonical Allele Identifier: CA2637631998
Gene: TCAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665245G>C , CM000679.2:g.39665245G>C GRCh38
NC_000017.10:g.37821498G>C , CM000679.1:g.37821498G>C GRCh37
NC_000017.9:g.35075024G>C NCBI36
NG_008892.1:g.4900G>C , LRG_210:g.4900G>C
NG_042278.1:g.2265G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-115G>C ENSP00000312624.2:n.-115G>C