Canonical Allele Identifier: CA1653130383
Gene:

Linked Data

dbSNP Id: rs1771941213

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.105805145T>A , CM000668.2:g.105805145T>A GRCh38
NC_000006.11:g.106253020T>A , CM000668.1:g.106253020T>A GRCh37
NC_000006.10:g.106359713T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_942835.1:n.510+24912A>T
XR_001744274.1:n.438+24912A>T
XR_001744275.1:n.337+24912A>T