Canonical Allele Identifier: CA2809442535
Gene: TCAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39664915T>C , CM000679.2:g.39664915T>C GRCh38
NC_000017.10:g.37821168T>C , CM000679.1:g.37821168T>C GRCh37
NC_000017.9:g.35074694T>C NCBI36
NG_008892.1:g.4570T>C , LRG_210:g.4570T>C
NG_042278.1:g.1935T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-445T>C ENSP00000312624.2:n.-445T>C