Canonical Allele Identifier: CA2470001200
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8605990C= , CM000686.2:g.8605990C= GRCh38
NC_000024.9:g.8474031C= , CM000686.1:g.8474031C= GRCh37
NC_000024.8:g.8534031C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000624507.1:c.53-959G= ENSP00000485522.1:n.53-959G=
ENST00000624593.1:c.92+16862G= ENSP00000485106.1:n.92+16862G=