Canonical Allele Identifier: CA2000590780
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112166883A= , CM000673.2:g.112166883A= GRCh38
NC_000011.9:g.112037606A= , CM000673.1:g.112037606A= GRCh37
NC_000011.8:g.111542816A= NCBI36
NG_028143.1:g.2235T=

Transcript Alleles

HGVS Amino-acid change
ENST00000525987.5:n.320-3536A=
ENST00000531744.5:c.315-3536A= ENSP00000456957.1:n.315-3536A=
ENST00000532699.1:c.315-3536A= ENSP00000456434.1:n.315-3536A=