Canonical Allele Identifier: CA59107096
Gene:

Linked Data

dbSNP Id: rs13020355

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870662T>C , CM000664.2:g.155870662T>C GRCh38
NC_000002.11:g.156727174T>C , CM000664.1:g.156727174T>C GRCh37
NC_000002.10:g.156435420T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923501.1:n.320-3475A>G
XR_001739749.1:n.331-29678A>G
XR_001739750.1:n.331-29678A>G
XR_001739751.1:n.331-29678A>G
XR_923501.2:n.331-3475A>G