Canonical Allele Identifier: CA2259200482
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs2057246569

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665341G>T , CM000679.2:g.39665341G>T GRCh38
NC_000017.10:g.37821594G>T , CM000679.1:g.37821594G>T GRCh37
NC_000017.9:g.35075120G>T NCBI36
NG_008892.1:g.4996G>T , LRG_210:g.4996G>T
NG_042278.1:g.2361G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000309889.2:c.-19G>T ENSP00000312624.2:n.-19G>T