Canonical Allele Identifier: CA2259200302
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs2057243829

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665020A>G , CM000679.2:g.39665020A>G GRCh38
NC_000017.10:g.37821273A>G , CM000679.1:g.37821273A>G GRCh37
NC_000017.9:g.35074799A>G NCBI36
NG_008892.1:g.4675A>G , LRG_210:g.4675A>G
NG_042278.1:g.2040A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-340A>G ENSP00000312624.2:n.-340A>G