Canonical Allele Identifier: CA2841191377
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56900018T>C , CM000667.2:g.56900018T>C GRCh38
NC_000005.9:g.56195845T>C , CM000667.1:g.56195845T>C GRCh37
NC_000005.8:g.56231602T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_948346.1:n.83-1722A>G
XR_948347.1:n.55A>G
XR_948347.3:n.385A>G