Canonical Allele Identifier: CA1339335835

Gene: AGXT

Linked Data

• dbSNP Id: rs1575712807

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240878185A>C , CM000664.2:g.240878185A>C	GRCh38
NC_000002.11:g.241817602A>C , CM000664.1:g.241817602A>C	GRCh37
NC_000002.10:g.241466275A>C	NCBI36
NG_008005.1:g.14441A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307503.4:c.1071+35A>C MANE Select	ENSP00000302620.3:n.1071+35A>C
ENST00000307503.3:c.1071+35A>C	ENSP00000302620.3:n.1071+35A>C
ENST00000470255.1:n.849+35A>C
NM_000030.2:c.1071+35A>C	NP_000021.1:n.1071+35A>C
NM_000030.3:c.1071+35A>C MANE Select	NP_000021.1:n.1071+35A>C