Canonical Allele Identifier: CA2824552545
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8707792A>T , CM000686.2:g.8707792A>T GRCh38
NC_000024.9:g.8575833A>T , CM000686.1:g.8575833A>T GRCh37
NC_000024.8:g.8635833A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000623558.1:c.139+8760A>T ENSP00000485446.1:n.139+8760A>T
ENST00000624593.1:c.-57+40924T>A ENSP00000485106.1:n.-57+40924T>A