Canonical Allele Identifier: CA1427019577
Gene: AHSG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186620636A= , CM000665.2:g.186620636A= GRCh38
NC_000003.11:g.186338425A= , CM000665.1:g.186338425A= GRCh37
NC_000003.10:g.187821119A= NCBI36
NG_011436.1:g.12576A=

Transcript Alleles

HGVS Amino-acid change
ENST00000411641.7:c.810A= MANE Select ENSP00000393887.2:p.Thr270=
ENST00000273784.5:c.813A= ENSP00000273784.5:p.Thr271=
ENST00000411641.6:c.810A= ENSP00000393887.2:p.Thr270=
NM_001622.2:c.810A= NP_001613.2:p.Thr270=
NM_001354571.1:c.813A= NP_001341500.1:p.Thr271=
NM_001354572.1:c.807A= NP_001341501.1:p.Thr269=
NM_001354573.1:c.726A= NP_001341502.1:p.Thr242=
NM_001622.3:c.810A= NP_001613.2:p.Thr270=
NM_001622.4:c.810A= MANE Select NP_001613.2:p.Thr270=
NM_001354571.2:c.813A= NP_001341500.1:p.Thr271=
NM_001354572.2:c.807A= NP_001341501.1:p.Thr269=
NM_001354573.2:c.726A= NP_001341502.1:p.Thr242=