Canonical Allele Identifier: CA2000590766
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112166853A= , CM000673.2:g.112166853A= GRCh38
NC_000011.9:g.112037576A= , CM000673.1:g.112037576A= GRCh37
NC_000011.8:g.111542786A= NCBI36
NG_028143.1:g.2265T=

Transcript Alleles

HGVS Amino-acid change
ENST00000525987.5:n.320-3566A=
ENST00000531744.5:c.315-3566A= ENSP00000456957.1:n.315-3566A=
ENST00000532699.1:c.315-3566A= ENSP00000456434.1:n.315-3566A=