Canonical Allele Identifier: CA1458504920
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54228598C= , CM000666.2:g.54228598C= GRCh38
NC_000004.11:g.55094765C= , CM000666.1:g.55094765C= GRCh37
NC_000004.10:g.54789522C= NCBI36
NG_009250.1:g.4502C= , LRG_309:g.4502C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000507166.5:c.1018-46327C= ENSP00000423325.1:n.1018-46327C=