Canonical Allele Identifier: CA1679711366
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.166038133G= , CM000668.2:g.166038133G= GRCh38
NC_000006.11:g.166451621G= , CM000668.1:g.166451621G= GRCh37
NC_000006.10:g.166371611G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943241.1:n.331+1576G=
XR_943241.2:n.334+1576G=