Canonical Allele Identifier: CA2269950690
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63498387T= , CM000679.2:g.63498387T= GRCh38
NC_000017.10:g.61575748T= , CM000679.1:g.61575748T= GRCh37
NC_000017.9:g.58929480T= NCBI36
NG_011648.1:g.26315T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000577647.2:c.1969+1402T= ENSP00000464149.1:n.1969+1402T=