Canonical Allele Identifier: CA59107098
Gene:

Linked Data

dbSNP Id: rs1030832329

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870669T>C , CM000664.2:g.155870669T>C GRCh38
NC_000002.11:g.156727181T>C , CM000664.1:g.156727181T>C GRCh37
NC_000002.10:g.156435427T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923501.1:n.320-3482A>G
XR_001739749.1:n.331-29685A>G
XR_001739750.1:n.331-29685A>G
XR_001739751.1:n.331-29685A>G
XR_923501.2:n.331-3482A>G