Canonical Allele Identifier: CA2744632032
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94564034T>C , CM000663.2:g.94564034T>C GRCh38
NC_000001.10:g.95029590T>C , CM000663.1:g.95029590T>C GRCh37
NC_000001.9:g.94802178T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001738161.1:n.461+421T>C