Canonical Allele Identifier: CA1438624535
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.11501991G= , CM000666.2:g.11501991G= GRCh38
NC_000004.11:g.11503615G= , CM000666.1:g.11503615G= GRCh37
NC_000004.10:g.11112713G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001741361.1:n.950+19145G=