Canonical Allele Identifier: CA2259200450
Gene: TCAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665299A= , CM000679.2:g.39665299A= GRCh38
NC_000017.10:g.37821552A= , CM000679.1:g.37821552A= GRCh37
NC_000017.9:g.35075078A= NCBI36
NG_008892.1:g.4954A= , LRG_210:g.4954A=
NG_042278.1:g.2319A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-61A= ENSP00000312624.2:n.-61A=