Canonical Allele Identifier: CA2259200258
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs2057243018

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39664929G>T , CM000679.2:g.39664929G>T GRCh38
NC_000017.10:g.37821182G>T , CM000679.1:g.37821182G>T GRCh37
NC_000017.9:g.35074708G>T NCBI36
NG_008892.1:g.4584G>T , LRG_210:g.4584G>T
NG_042278.1:g.1949G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-431G>T ENSP00000312624.2:n.-431G>T