Canonical Allele Identifier: CA1284431638
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122368830G= , CM000664.2:g.122368830G= GRCh38
NC_000002.11:g.123126406G= , CM000664.1:g.123126406G= GRCh37
NC_000002.10:g.122842876G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923278.1:n.556-24133G=
XR_001739684.1:n.556-24133G=