Canonical Allele Identifier: CA1458504732
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54228388C= , CM000666.2:g.54228388C= GRCh38
NC_000004.11:g.55094555C= , CM000666.1:g.55094555C= GRCh37
NC_000004.10:g.54789312C= NCBI36
NG_009250.1:g.4292C= , LRG_309:g.4292C=

Transcript Alleles

HGVS Amino-acid change
ENST00000507166.5:c.1018-46537C= ENSP00000423325.1:n.1018-46537C=