Canonical Allele Identifier: CA1427016911
Gene: AHSG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186614783C= , CM000665.2:g.186614783C= GRCh38
NC_000003.11:g.186332572C= , CM000665.1:g.186332572C= GRCh37
NC_000003.10:g.187815266C= NCBI36
NG_011436.1:g.6723C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000411641.7:c.214-902C= MANE Select ENSP00000393887.2:n.214-902C=
ENST00000273784.5:c.214-902C= ENSP00000273784.5:n.214-902C=
ENST00000411641.6:c.214-902C= ENSP00000393887.2:n.214-902C=
ENST00000478441.1:n.271-902C=
NM_001622.2:c.214-902C= NP_001613.2:n.214-902C=
NM_001354571.1:c.214-902C= NP_001341500.1:n.214-902C=
NM_001354572.1:c.214-905C= NP_001341501.1:n.214-905C=
NM_001354573.1:c.214-902C= NP_001341502.1:n.214-902C=
NM_001622.3:c.214-902C= NP_001613.2:n.214-902C=
NM_001622.4:c.214-902C= MANE Select NP_001613.2:n.214-902C=
NM_001354571.2:c.214-902C= NP_001341500.1:n.214-902C=
NM_001354572.2:c.214-905C= NP_001341501.1:n.214-905C=
NM_001354573.2:c.214-902C= NP_001341502.1:n.214-902C=