Canonical Allele Identifier: CA2259200479
Gene: TCAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665340A= , CM000679.2:g.39665340A= GRCh38
NC_000017.10:g.37821593A= , CM000679.1:g.37821593A= GRCh37
NC_000017.9:g.35075119A= NCBI36
NG_008892.1:g.4995A= , LRG_210:g.4995A=
NG_042278.1:g.2360A=

Transcript Alleles

HGVS Amino-acid change
ENST00000309889.2:c.-20A= ENSP00000312624.2:n.-20A=