Canonical Allele Identifier: CA2000589932
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112164639A= , CM000673.2:g.112164639A= GRCh38
NC_000011.9:g.112035362A= , CM000673.1:g.112035362A= GRCh37
NC_000011.8:g.111540572A= NCBI36
NG_028143.1:g.4479T=

Transcript Alleles

HGVS Amino-acid change
ENST00000525987.5:n.320-5780A=
ENST00000531744.5:c.315-5780A= ENSP00000456957.1:n.315-5780A=
ENST00000532699.1:c.315-5780A= ENSP00000456434.1:n.315-5780A=