Canonical Allele Identifier: CA1300258850
Gene:

Linked Data

dbSNP Id: rs1683152548

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870700A>G , CM000664.2:g.155870700A>G GRCh38
NC_000002.11:g.156727212A>G , CM000664.1:g.156727212A>G GRCh37
NC_000002.10:g.156435458A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923501.1:n.320-3513T>C
XR_001739749.1:n.331-29716T>C
XR_001739750.1:n.331-29716T>C
XR_001739751.1:n.331-29716T>C
XR_923501.2:n.331-3513T>C