Canonical Allele Identifier: CA1247519203
Gene:

Linked Data

dbSNP Id: rs1667993521

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.41534782C>G , CM000664.2:g.41534782C>G GRCh38
NC_000002.11:g.41761922C>G , CM000664.1:g.41761922C>G GRCh37
NC_000002.10:g.41615426C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939996.1:n.181+2944G>C
XR_939997.1:n.146+2944G>C
XR_939997.2:n.9529+2944G>C