Canonical Allele Identifier: CA1762609665
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.9400136T= , CM000670.2:g.9400136T= GRCh38
NC_000008.10:g.9257646T= , CM000670.1:g.9257646T= GRCh37
NC_000008.9:g.9295056T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948936.1:n.185+3809A=
XR_948940.1:n.96-3727T=
XR_948941.1:n.96-13513T=
XR_002956685.1:n.99-3727T=
XR_948940.2:n.99-3727T=
XR_948941.2:n.99-13513T=