Canonical Allele Identifier: CA2259200266
Gene: TCAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39664953A= , CM000679.2:g.39664953A= GRCh38
NC_000017.10:g.37821206A= , CM000679.1:g.37821206A= GRCh37
NC_000017.9:g.35074732A= NCBI36
NG_008892.1:g.4608A= , LRG_210:g.4608A=
NG_042278.1:g.1973A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-407A= ENSP00000312624.2:n.-407A=