Canonical Allele Identifier: CA2259200444
Gene: TCAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665283C= , CM000679.2:g.39665283C= GRCh38
NC_000017.10:g.37821536C= , CM000679.1:g.37821536C= GRCh37
NC_000017.9:g.35075062C= NCBI36
NG_008892.1:g.4938C= , LRG_210:g.4938C=
NG_042278.1:g.2303C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-77C= ENSP00000312624.2:n.-77C=