Canonical Allele Identifier: CA1427018566
Gene: AHSG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186618238T= , CM000665.2:g.186618238T= GRCh38
NC_000003.11:g.186336027T= , CM000665.1:g.186336027T= GRCh37
NC_000003.10:g.187818721T= NCBI36
NG_011436.1:g.10178T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000411641.7:c.574-298T= MANE Select ENSP00000393887.2:n.574-298T=
ENST00000273784.5:c.577-298T= ENSP00000273784.5:n.577-298T=
ENST00000411641.6:c.574-298T= ENSP00000393887.2:n.574-298T=
NM_001622.2:c.574-298T= NP_001613.2:n.574-298T=
NM_001354571.1:c.577-298T= NP_001341500.1:n.577-298T=
NM_001354572.1:c.571-298T= NP_001341501.1:n.571-298T=
NM_001354573.1:c.574-298T= NP_001341502.1:n.574-298T=
NM_001622.3:c.574-298T= NP_001613.2:n.574-298T=
NM_001622.4:c.574-298T= MANE Select NP_001613.2:n.574-298T=
NM_001354571.2:c.577-298T= NP_001341500.1:n.577-298T=
NM_001354572.2:c.571-298T= NP_001341501.1:n.571-298T=
NM_001354573.2:c.574-298T= NP_001341502.1:n.574-298T=