Canonical Allele Identifier: CA1247518980
Gene:

Linked Data

dbSNP Id: rs1667988829

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.41534441T>C , CM000664.2:g.41534441T>C GRCh38
NC_000002.11:g.41761581T>C , CM000664.1:g.41761581T>C GRCh37
NC_000002.10:g.41615085T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939996.1:n.181+3285A>G
XR_939997.1:n.146+3285A>G
XR_939997.2:n.9529+3285A>G