Canonical Allele Identifier: CA2581826828
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122368903A>T , CM000664.2:g.122368903A>T GRCh38
NC_000002.11:g.123126479A>T , CM000664.1:g.123126479A>T GRCh37
NC_000002.10:g.122842949A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923278.1:n.556-24060A>T
XR_001739684.1:n.556-24060A>T