Canonical Allele Identifier: CA2269950691
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63498388T= , CM000679.2:g.63498388T= GRCh38
NC_000017.10:g.61575749T= , CM000679.1:g.61575749T= GRCh37
NC_000017.9:g.58929481T= NCBI36
NG_011648.1:g.26316T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000577647.2:c.1969+1403T= ENSP00000464149.1:n.1969+1403T=