Canonical Allele Identifier: CA1339335236

Gene: AGXT

Linked Data

• dbSNP Id: rs2059028249

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240877067G>C , CM000664.2:g.240877067G>C	GRCh38
NC_000002.11:g.241816484G>C , CM000664.1:g.241816484G>C	GRCh37
NC_000002.10:g.241465157G>C	NCBI36
NG_008005.1:g.13323G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307503.4:c.847-470G>C MANE Select	ENSP00000302620.3:n.847-470G>C
ENST00000307503.3:c.847-470G>C	ENSP00000302620.3:n.847-470G>C
ENST00000470255.1:n.155G>C
NM_000030.2:c.847-470G>C	NP_000021.1:n.847-470G>C
NM_000030.3:c.847-470G>C MANE Select	NP_000021.1:n.847-470G>C