Canonical Allele Identifier: CA437357940

Gene: AHSG

Linked Data

• dbSNP Id: rs772452989
• MyVariant Identifiers: chr3:g.186336402C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186618613C>T , CM000665.2:g.186618613C>T	GRCh38
NC_000003.11:g.186336402C>T , CM000665.1:g.186336402C>T	GRCh37
NC_000003.10:g.187819096C>T	NCBI36
NG_011436.1:g.10553C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.651C>T MANE Select	ENSP00000393887.2:p.Ala217=
ENST00000273784.5:c.654C>T	ENSP00000273784.5:p.Ala218=
ENST00000411641.6:c.651C>T	ENSP00000393887.2:p.Ala217=
NM_001622.2:c.651C>T	NP_001613.2:p.Ala217=
NM_001354571.1:c.654C>T	NP_001341500.1:p.Ala218=
NM_001354572.1:c.648C>T	NP_001341501.1:p.Ala216=
NM_001354573.1:c.651C>T	NP_001341502.1:p.Ala217=
NM_001622.3:c.651C>T	NP_001613.2:p.Ala217=
NM_001622.4:c.651C>T MANE Select	NP_001613.2:p.Ala217=
NM_001354571.2:c.654C>T	NP_001341500.1:p.Ala218=
NM_001354572.2:c.648C>T	NP_001341501.1:p.Ala216=
NM_001354573.2:c.651C>T	NP_001341502.1:p.Ala217=