Canonical Allele Identifier: CA1762609727
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.9400232T= , CM000670.2:g.9400232T= GRCh38
NC_000008.10:g.9257742T= , CM000670.1:g.9257742T= GRCh37
NC_000008.9:g.9295152T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948936.1:n.185+3713A=
XR_948940.1:n.96-3631T=
XR_948941.1:n.96-13417T=
XR_002956685.1:n.99-3631T=
XR_948940.2:n.99-3631T=
XR_948941.2:n.99-13417T=