Canonical Allele Identifier: CA1672979269
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151633711G= , CM000668.2:g.151633711G= GRCh38
NC_000006.11:g.151954846G= , CM000668.1:g.151954846G= GRCh37
NC_000006.10:g.151996539G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943115.1:n.2496+3729G=