Canonical Allele Identifier: CA1762609749
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.9400274T= , CM000670.2:g.9400274T= GRCh38
NC_000008.10:g.9257784T= , CM000670.1:g.9257784T= GRCh37
NC_000008.9:g.9295194T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948936.1:n.185+3671A=
XR_948940.1:n.96-3589T=
XR_948941.1:n.96-13375T=
XR_002956685.1:n.99-3589T=
XR_948940.2:n.99-3589T=
XR_948941.2:n.99-13375T=