Canonical Allele Identifier: CA2699207837
Gene:

Linked Data

dbSNP Id: rs2103837548

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.41534510G>C , CM000664.2:g.41534510G>C GRCh38
NC_000002.11:g.41761650G>C , CM000664.1:g.41761650G>C GRCh37
NC_000002.10:g.41615154G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939996.1:n.181+3216C>G
XR_939997.1:n.146+3216C>G
XR_939997.2:n.9529+3216C>G