Canonical Allele Identifier: CA437358402

Gene: AHSG

Linked Data

• dbSNP Id: rs1716455417
• gnomAD v3: 3-186620657-A-T
• gnomAD v4: 3-186620657-A-T
• MyVariant Identifiers: chr3:g.186338446A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186620657A>T , CM000665.2:g.186620657A>T	GRCh38
NC_000003.11:g.186338446A>T , CM000665.1:g.186338446A>T	GRCh37
NC_000003.10:g.187821140A>T	NCBI36
NG_011436.1:g.12597A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.831A>T MANE Select	ENSP00000393887.2:p.Ala277=
ENST00000273784.5:c.834A>T	ENSP00000273784.5:p.Ala278=
ENST00000411641.6:c.831A>T	ENSP00000393887.2:p.Ala277=
NM_001622.2:c.831A>T	NP_001613.2:p.Ala277=
NM_001354571.1:c.834A>T	NP_001341500.1:p.Ala278=
NM_001354572.1:c.828A>T	NP_001341501.1:p.Ala276=
NM_001354573.1:c.747A>T	NP_001341502.1:p.Ala249=
NM_001622.3:c.831A>T	NP_001613.2:p.Ala277=
NM_001622.4:c.831A>T MANE Select	NP_001613.2:p.Ala277=
NM_001354571.2:c.834A>T	NP_001341500.1:p.Ala278=
NM_001354572.2:c.828A>T	NP_001341501.1:p.Ala276=
NM_001354573.2:c.747A>T	NP_001341502.1:p.Ala249=