Canonical Allele Identifier: CA1605795002
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1535612T= , CM000668.2:g.1535612T= GRCh38
NC_000006.11:g.1535847T= , CM000668.1:g.1535847T= GRCh37
NC_000006.10:g.1480846T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427861.2:n.234+16734A=
XR_926380.1:n.218-2844T=
XR_926381.1:n.1108-2844T=
XR_926382.1:n.235-6433A=
XR_926384.1:n.200-6433A=
XR_001743921.1:n.235-6457A=
XR_427861.3:n.234+16734A=
XR_926381.2:n.1123-2844T=