Canonical Allele Identifier: CA163356
Gene: AHSG HGNC NCBI

Linked Data

ClinVar Variation Id: 126866
ClinVar RCV Id: RCV000128584
dbSNP Id: rs2070635

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186618387A>G , CM000665.2:g.186618387A>G GRCh38
NC_000003.11:g.186336176A>G , CM000665.1:g.186336176A>G GRCh37
NC_000003.10:g.187818870A>G NCBI36
NG_011436.1:g.10327A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000411641.7:c.574-149A>G MANE Select ENSP00000393887.2:n.574-149A>G
ENST00000273784.5:c.577-149A>G ENSP00000273784.5:n.577-149A>G
ENST00000411641.6:c.574-149A>G ENSP00000393887.2:n.574-149A>G
NM_001622.2:c.574-149A>G NP_001613.2:n.574-149A>G
NM_001354571.1:c.577-149A>G NP_001341500.1:n.577-149A>G
NM_001354572.1:c.571-149A>G NP_001341501.1:n.571-149A>G
NM_001354573.1:c.574-149A>G NP_001341502.1:n.574-149A>G
NM_001622.3:c.574-149A>G NP_001613.2:n.574-149A>G
NM_001622.4:c.574-149A>G MANE Select NP_001613.2:n.574-149A>G
NM_001354571.2:c.577-149A>G NP_001341500.1:n.577-149A>G
NM_001354572.2:c.571-149A>G NP_001341501.1:n.571-149A>G
NM_001354573.2:c.574-149A>G NP_001341502.1:n.574-149A>G