Canonical Allele Identifier: CA288175019
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.15922707A>C , CM000679.2:g.15922707A>C GRCh38
NC_000017.10:g.15826021A>C , CM000679.1:g.15826021A>C GRCh37
NC_000017.9:g.15766746A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011524118.1:c.349-3436A>C XP_011522420.1:n.349-3436A>C