Canonical Allele Identifier: CA1659692047
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.121837133C= , CM000668.2:g.121837133C= GRCh38
NC_000006.11:g.122158279C= , CM000668.1:g.122158279C= GRCh37
NC_000006.10:g.122199978C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_942936.1:n.241-20778C=
XR_942937.1:n.240+69518C=
XR_942938.1:n.241-20778C=
XR_942939.1:n.241-20778C=
XR_942940.1:n.241-20778C=
XR_942941.1:n.241-20778C=
XR_942936.2:n.241-20778C=
XR_942937.3:n.240+69518C=