Canonical Allele Identifier: CA2000589931
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112164638G= , CM000673.2:g.112164638G= GRCh38
NC_000011.9:g.112035361G= , CM000673.1:g.112035361G= GRCh37
NC_000011.8:g.111540571G= NCBI36
NG_028143.1:g.4480C=

Transcript Alleles

HGVS Amino-acid change
ENST00000525987.5:n.320-5781G=
ENST00000531744.5:c.315-5781G= ENSP00000456957.1:n.315-5781G=
ENST00000532699.1:c.315-5781G= ENSP00000456434.1:n.315-5781G=