Canonical Allele Identifier: CA11390342
Gene: AHSG HGNC NCBI
MyVariant.info:
GRCh38 chr3:g.186620038T>C
GRCh37 chr3:g.186337827T>C
gnomAD v2:
3:186337827 T / C
gnomAD v3:
3:186620038 T / C
gnomAD v4:
chr3-186620038-T-C
Joint Max Group AF 0.57922713 (EAS)
Genomes Max Group AF 0.59425711 (EAS)
Exomes Max Group AF 0.57464833 (EAS)
dbSNP:
2518136
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186620038T>C , CM000665.2:g.186620038T>C GRCh38
NC_000003.11:g.186337827T>C , CM000665.1:g.186337827T>C GRCh37
NC_000003.10:g.187820521T>C NCBI36
NG_011436.1:g.11978T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000411641.7:c.759+98T>C MANE Select ENSP00000393887.2:n.759+98T>C
ENST00000273784.5:c.762+98T>C ENSP00000273784.5:n.762+98T>C
ENST00000411641.6:c.759+98T>C ENSP00000393887.2:n.759+98T>C
NM_001622.2:c.759+98T>C NP_001613.2:n.759+98T>C
NM_001354571.1:c.762+98T>C NP_001341500.1:n.762+98T>C
NM_001354572.1:c.756+98T>C NP_001341501.1:n.756+98T>C
NM_001354573.1:c.676-548T>C NP_001341502.1:n.676-548T>C
NM_001622.3:c.759+98T>C NP_001613.2:n.759+98T>C
NM_001622.4:c.759+98T>C MANE Select NP_001613.2:n.759+98T>C
NM_001354571.2:c.762+98T>C NP_001341500.1:n.762+98T>C
NM_001354572.2:c.756+98T>C NP_001341501.1:n.756+98T>C
NM_001354573.2:c.676-548T>C NP_001341502.1:n.676-548T>C
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