Canonical Allele Identifier: CA1557963419
Gene:

Linked Data

dbSNP Id: rs1753647180

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.79549960A>G , CM000667.2:g.79549960A>G GRCh38
NC_000005.9:g.78845783A>G , CM000667.1:g.78845783A>G GRCh37
NC_000005.8:g.78881539A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948497.1:n.72+2316A>G
XR_948498.1:n.159+2123A>G
XR_948499.1:n.67+1658A>G
XR_948497.2:n.72+2316A>G
XR_948498.2:n.159+2123A>G
XR_948499.2:n.225+1658A>G