Canonical Allele Identifier: CA1448129

Gene: AGT

Linked Data

• dbSNP Id: rs771127679
• ExAC: 1:230840130 G / A
• gnomAD v2: 1-230840130-G-A
• MyVariant Identifiers: chr1:g.230840130G>A (hg19) ; chr1:g.230704384G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230704384G>A , CM000663.2:g.230704384G>A	GRCh38
NC_000001.10:g.230840130G>A , CM000663.1:g.230840130G>A	GRCh37
NC_000001.9:g.228906753G>A	NCBI36
NG_008836.1:g.15207C>T
NG_008836.2:g.15207C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.1098-47C>T MANE Select	ENSP00000355627.5:n.1098-47C>T
ENST00000679684.1:c.1098-47C>T	ENSP00000505981.1:n.1098-47C>T
ENST00000679738.1:c.1098-47C>T	ENSP00000505063.1:n.1098-47C>T
ENST00000679802.1:c.*557-47C>T	ENSP00000505184.1:n.*557-47C>T
ENST00000679854.1:n.5403-47C>T
ENST00000679957.1:c.1098-47C>T	ENSP00000506646.1:n.1098-47C>T
ENST00000680041.1:c.1098-47C>T	ENSP00000504866.1:n.1098-47C>T
ENST00000680783.1:c.829+5611C>T	ENSP00000506329.1:n.829+5611C>T
ENST00000681269.1:c.1098-47C>T	ENSP00000505985.1:n.1098-47C>T
ENST00000681347.1:n.3157C>T
ENST00000681514.1:c.1098-47C>T	ENSP00000505963.1:n.1098-47C>T
ENST00000681772.1:c.*592-47C>T	ENSP00000505829.1:n.*592-47C>T
ENST00000366667.4:c.1125-47C>T	ENSP00000355627.4:n.1125-47C>T
NM_000029.3:c.1125-47C>T	NP_000020.1:n.1125-47C>T
NM_000029.4:c.1125-47C>T	NP_000020.1:n.1125-47C>T
NM_001382817.3:c.1098-47C>T	NP_001369746.2:n.1098-47C>T
NM_001384479.1:c.1098-47C>T MANE Select	NP_001371408.1:n.1098-47C>T