Canonical Allele Identifier: CA1339336001

Gene: AGXT

Linked Data

• dbSNP Id: rs2059040162

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240878468G>C , CM000664.2:g.240878468G>C	GRCh38
NC_000002.11:g.241817885G>C , CM000664.1:g.241817885G>C	GRCh37
NC_000002.10:g.241466558G>C	NCBI36
NG_008005.1:g.14724G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307503.4:c.1072-246G>C MANE Select	ENSP00000302620.3:n.1072-246G>C
ENST00000307503.3:c.1072-246G>C	ENSP00000302620.3:n.1072-246G>C
ENST00000470255.1:n.850-246G>C
NM_000030.2:c.1072-246G>C	NP_000021.1:n.1072-246G>C
NM_000030.3:c.1072-246G>C MANE Select	NP_000021.1:n.1072-246G>C