Canonical Allele Identifier: CA2568236622
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54228488C>A , CM000666.2:g.54228488C>A GRCh38
NC_000004.11:g.55094655C>A , CM000666.1:g.55094655C>A GRCh37
NC_000004.10:g.54789412C>A NCBI36
NG_009250.1:g.4392C>A , LRG_309:g.4392C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000507166.5:c.1018-46437C>A ENSP00000423325.1:n.1018-46437C>A