Canonical Allele Identifier: CA1458504693
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54228333G= , CM000666.2:g.54228333G= GRCh38
NC_000004.11:g.55094500G= , CM000666.1:g.55094500G= GRCh37
NC_000004.10:g.54789257G= NCBI36
NG_009250.1:g.4237G= , LRG_309:g.4237G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000507166.5:c.1018-46592G= ENSP00000423325.1:n.1018-46592G=