Canonical Allele Identifier: CA2668958752
Gene: AHSG HGNC NCBI

Linked Data

gnomAD v4: 3-186618395-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186618395C>A , CM000665.2:g.186618395C>A GRCh38
NC_000003.11:g.186336184C>A , CM000665.1:g.186336184C>A GRCh37
NC_000003.10:g.187818878C>A NCBI36
NG_011436.1:g.10335C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000411641.7:c.574-141C>A MANE Select ENSP00000393887.2:n.574-141C>A
ENST00000273784.5:c.577-141C>A ENSP00000273784.5:n.577-141C>A
ENST00000411641.6:c.574-141C>A ENSP00000393887.2:n.574-141C>A
NM_001622.2:c.574-141C>A NP_001613.2:n.574-141C>A
NM_001354571.1:c.577-141C>A NP_001341500.1:n.577-141C>A
NM_001354572.1:c.571-141C>A NP_001341501.1:n.571-141C>A
NM_001354573.1:c.574-141C>A NP_001341502.1:n.574-141C>A
NM_001622.3:c.574-141C>A NP_001613.2:n.574-141C>A
NM_001622.4:c.574-141C>A MANE Select NP_001613.2:n.574-141C>A
NM_001354571.2:c.577-141C>A NP_001341500.1:n.577-141C>A
NM_001354572.2:c.571-141C>A NP_001341501.1:n.571-141C>A
NM_001354573.2:c.574-141C>A NP_001341502.1:n.574-141C>A
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