Canonical Allele Identifier: CA2637632106
Gene: TCAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665325A>G , CM000679.2:g.39665325A>G GRCh38
NC_000017.10:g.37821578A>G , CM000679.1:g.37821578A>G GRCh37
NC_000017.9:g.35075104A>G NCBI36
NG_008892.1:g.4980A>G , LRG_210:g.4980A>G
NG_042278.1:g.2345A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000309889.2:c.-35A>G ENSP00000312624.2:n.-35A>G