Canonical Allele Identifier: CA1659692061
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.121837178A= , CM000668.2:g.121837178A= GRCh38
NC_000006.11:g.122158324A= , CM000668.1:g.122158324A= GRCh37
NC_000006.10:g.122200023A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_942936.1:n.241-20733A=
XR_942937.1:n.240+69563A=
XR_942938.1:n.241-20733A=
XR_942939.1:n.241-20733A=
XR_942940.1:n.241-20733A=
XR_942941.1:n.241-20733A=
XR_942936.2:n.241-20733A=
XR_942937.3:n.240+69563A=