Canonical Allele Identifier: CA2485026942
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.211379671T= , CM000663.2:g.211379671T= GRCh38
NC_000001.10:g.211553013T= , CM000663.1:g.211553013T= GRCh37
NC_000001.9:g.209619636T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001738446.1:n.291+2524A=