Canonical Allele Identifier: CA2269950707
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63498412G= , CM000679.2:g.63498412G= GRCh38
NC_000017.10:g.61575773G= , CM000679.1:g.61575773G= GRCh37
NC_000017.9:g.58929505G= NCBI36
NG_011648.1:g.26340G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000577647.2:c.1969+1427G= ENSP00000464149.1:n.1969+1427G=