Canonical Allele Identifier: CA2000590041
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112164880T= , CM000673.2:g.112164880T= GRCh38
NC_000011.9:g.112035603T= , CM000673.1:g.112035603T= GRCh37
NC_000011.8:g.111540813T= NCBI36
NG_028143.1:g.4238A=

Transcript Alleles

HGVS Amino-acid change
ENST00000525987.5:n.320-5539T=
ENST00000531744.5:c.315-5539T= ENSP00000456957.1:n.315-5539T=
ENST00000532699.1:c.315-5539T= ENSP00000456434.1:n.315-5539T=