Canonical Allele Identifier: CA1659692000
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.121837047A= , CM000668.2:g.121837047A= GRCh38
NC_000006.11:g.122158193A= , CM000668.1:g.122158193A= GRCh37
NC_000006.10:g.122199892A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_942936.1:n.241-20864A=
XR_942937.1:n.240+69432A=
XR_942938.1:n.241-20864A=
XR_942939.1:n.241-20864A=
XR_942940.1:n.241-20864A=
XR_942941.1:n.241-20864A=
XR_942936.2:n.241-20864A=
XR_942937.3:n.240+69432A=