Canonical Allele Identifier: CA2824549878
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8606170G>C , CM000686.2:g.8606170G>C GRCh38
NC_000024.9:g.8474211G>C , CM000686.1:g.8474211G>C GRCh37
NC_000024.8:g.8534211G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000624507.1:c.53-1139C>G ENSP00000485522.1:n.53-1139C>G
ENST00000624593.1:c.92+16682C>G ENSP00000485106.1:n.92+16682C>G