Canonical Allele Identifier: CA2470001214
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8606182T= , CM000686.2:g.8606182T= GRCh38
NC_000024.9:g.8474223T= , CM000686.1:g.8474223T= GRCh37
NC_000024.8:g.8534223T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000624507.1:c.53-1151A= ENSP00000485522.1:n.53-1151A=
ENST00000624593.1:c.92+16670A= ENSP00000485106.1:n.92+16670A=