Canonical Allele Identifier: CA2330336232
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.28544569T= , CM000681.2:g.28544569T= GRCh38
NC_000019.9:g.29035476T= , CM000681.1:g.29035476T= GRCh37
NC_000019.8:g.33727316T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110759.1:n.657-77789A=
XR_243979.1:n.110-51546A=