Canonical Allele Identifier: CA2271197628
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240104A>G , CM000679.2:g.66240104A>G GRCh38
NC_000017.10:g.64236222A>G , CM000679.1:g.64236222A>G GRCh37
NC_000017.9:g.61666684A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000577982.1:c.-43-10682T>C ENSP00000464301.1:p.=