Canonical Allele Identifier: CA2581562576
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31440488C>T , CM000668.2:g.31440488C>T GRCh38
NC_000006.11:g.31408265C>T , CM000668.1:g.31408265C>T GRCh37
NC_000006.10:g.31516244C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926694.1:n.54+372G>A