Canonical Allele Identifier: CA290433606
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs191036015
MyVariant Identifiers: chr17:g.37821575T>A (hg19) chr17:g.39665322T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665322T>A , CM000679.2:g.39665322T>A GRCh38
NC_000017.10:g.37821575T>A , CM000679.1:g.37821575T>A GRCh37
NC_000017.9:g.35075101T>A NCBI36
NG_008892.1:g.4977T>A , LRG_210:g.4977T>A
NG_042278.1:g.2342T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-38T>A ENSP00000312624.2:n.-38T>A
Search 100 bp 5'
Search 100 bp 3'