Canonical Allele Identifier: CA2824549880
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8606175A>G , CM000686.2:g.8606175A>G GRCh38
NC_000024.9:g.8474216A>G , CM000686.1:g.8474216A>G GRCh37
NC_000024.8:g.8534216A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000624507.1:c.53-1144T>C ENSP00000485522.1:n.53-1144T>C
ENST00000624593.1:c.92+16677T>C ENSP00000485106.1:n.92+16677T>C