Canonical Allele Identifier: CA1552561709
Gene:

Linked Data

dbSNP Id: rs968685958

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.66487817T>C , CM000667.2:g.66487817T>C GRCh38
NC_000005.9:g.65783645T>C , CM000667.1:g.65783645T>C GRCh37
NC_000005.8:g.65819401T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_948381.1:n.649-49019T>C