Canonical Allele Identifier: CA2842289613
Gene: TCAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665327G>T , CM000679.2:g.39665327G>T GRCh38
NC_000017.10:g.37821580G>T , CM000679.1:g.37821580G>T GRCh37
NC_000017.9:g.35075106G>T NCBI36
NG_008892.1:g.4982G>T , LRG_210:g.4982G>T
NG_042278.1:g.2347G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-33G>T ENSP00000312624.2:n.-33G>T