Canonical Allele Identifier: CA1605795121
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1535935G= , CM000668.2:g.1535935G= GRCh38
NC_000006.11:g.1536170G= , CM000668.1:g.1536170G= GRCh37
NC_000006.10:g.1481169G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427861.2:n.234+16411C=
XR_926380.1:n.218-2521G=
XR_926381.1:n.1108-2521G=
XR_926382.1:n.235-6756C=
XR_926384.1:n.200-6756C=
XR_001743921.1:n.235-6780C=
XR_427861.3:n.234+16411C=
XR_926381.2:n.1123-2521G=