Canonical Allele Identifier: CA1475317289
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89681893A= , CM000666.2:g.89681893A= GRCh38
NC_000004.11:g.90603044A= , CM000666.1:g.90603044A= GRCh37
NC_000004.10:g.90822067A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001741765.1:n.228+213A=
XR_001741766.1:n.232+209A=
XR_938984.1:n.210+209A=
XR_938984.2:n.232+209A=
XR_938985.1:n.210+209A=
XR_938985.2:n.232+209A=
XR_938986.1:n.435-9392A=
XR_938986.2:n.460-9392A=
XR_938987.1:n.689-9392A=
XR_938987.2:n.749-9392A=
XR_938988.1:n.555-9392A=
XR_938989.1:n.210+209A=
XR_938989.2:n.232+209A=
XR_938990.1:n.299-9392A=
XR_938991.1:n.435-37933A=
XR_938993.1:n.210+209A=
XR_938994.1:n.780-9392A=
XR_938995.1:n.614-9392A=