Canonical Allele Identifier: CA2269950695
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63498398G= , CM000679.2:g.63498398G= GRCh38
NC_000017.10:g.61575759G= , CM000679.1:g.61575759G= GRCh37
NC_000017.9:g.58929491G= NCBI36
NG_011648.1:g.26326G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000577647.2:c.1969+1413G= ENSP00000464149.1:n.1969+1413G=