Canonical Allele Identifier: CA1247519082
Gene:

Linked Data

dbSNP Id: rs1667990809

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.41534610G>A , CM000664.2:g.41534610G>A GRCh38
NC_000002.11:g.41761750G>A , CM000664.1:g.41761750G>A GRCh37
NC_000002.10:g.41615254G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939996.1:n.181+3116C>T
XR_939997.1:n.146+3116C>T
XR_939997.2:n.9529+3116C>T