Canonical Allele Identifier: CA1427016921
Gene: AHSG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186614797G= , CM000665.2:g.186614797G= GRCh38
NC_000003.11:g.186332586G= , CM000665.1:g.186332586G= GRCh37
NC_000003.10:g.187815280G= NCBI36
NG_011436.1:g.6737G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000411641.7:c.214-888G= MANE Select ENSP00000393887.2:n.214-888G=
ENST00000273784.5:c.214-888G= ENSP00000273784.5:n.214-888G=
ENST00000411641.6:c.214-888G= ENSP00000393887.2:n.214-888G=
ENST00000478441.1:n.271-888G=
NM_001622.2:c.214-888G= NP_001613.2:n.214-888G=
NM_001354571.1:c.214-888G= NP_001341500.1:n.214-888G=
NM_001354572.1:c.214-891G= NP_001341501.1:n.214-891G=
NM_001354573.1:c.214-888G= NP_001341502.1:n.214-888G=
NM_001622.3:c.214-888G= NP_001613.2:n.214-888G=
NM_001622.4:c.214-888G= MANE Select NP_001613.2:n.214-888G=
NM_001354571.2:c.214-888G= NP_001341500.1:n.214-888G=
NM_001354572.2:c.214-891G= NP_001341501.1:n.214-891G=
NM_001354573.2:c.214-888G= NP_001341502.1:n.214-888G=