Canonical Allele Identifier: CA1595158933
Gene:

Linked Data

dbSNP Id: rs1757449206

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159580613A>G , CM000667.2:g.159580613A>G GRCh38
NC_000005.9:g.159007621A>G , CM000667.1:g.159007621A>G GRCh37
NC_000005.8:g.158940199A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_941139.1:n.2075+178A>G
XR_941140.1:n.2075+178A>G
XR_941141.1:n.570+178A>G
XR_941139.2:n.2229+178A>G