Canonical Allele Identifier: CA1610684927
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.11943618G= , CM000668.2:g.11943618G= GRCh38
NC_000006.11:g.11943851G= , CM000668.1:g.11943851G= GRCh37
NC_000006.10:g.12051837G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001743976.1:n.348-7917G=