Canonical Allele Identifier: CA1147240318
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.224887092C= , CM000663.2:g.224887092C= GRCh38
NC_000001.10:g.225074794C= , CM000663.1:g.225074794C= GRCh37
NC_000001.9:g.223141417C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949207.1:n.66-2311G=
XR_949207.2:n.63-2311G=