Canonical Allele Identifier: CA1818161788
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127012626T= , CM000670.2:g.127012626T= GRCh38
NC_000008.10:g.128024871T= , CM000670.1:g.128024871T= GRCh37
NC_000008.9:g.128094053T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746076.2:n.1364+6008T=