Canonical Allele Identifier: CA1149396867
Gene:

Linked Data

dbSNP Id: rs1659179345

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2036373A>G , CM000663.2:g.2036373A>G GRCh38
NC_000001.10:g.1967812A>G , CM000663.1:g.1967812A>G GRCh37
NC_000001.9:g.1957672A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_946823.1:n.773+62T>C
XR_001737845.2:n.838T>C
XR_946823.3:n.776+62T>C