Canonical Allele Identifier: CA2747669400
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.213682248C>G , CM000663.2:g.213682248C>G GRCh38
NC_000001.10:g.213855591C>G , CM000663.1:g.213855591C>G GRCh37
NC_000001.9:g.211922214C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001738463.1:n.601-49169C>G
XR_001738464.1:n.426-49169C>G