Canonical Allele Identifier: CA1339332062

Gene: AGXT

Linked Data

• dbSNP Id: rs1575708406

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240871323A>C , CM000664.2:g.240871323A>C	GRCh38
NC_000002.11:g.241810740A>C , CM000664.1:g.241810740A>C	GRCh37
NC_000002.10:g.241459413A>C	NCBI36
NG_008005.1:g.7579A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307503.4:c.424-26A>C MANE Select	ENSP00000302620.3:n.424-26A>C
ENST00000307503.3:c.424-26A>C	ENSP00000302620.3:n.424-26A>C
ENST00000472436.1:n.444-26A>C
ENST00000476698.1:n.135A>C
NM_000030.2:c.424-26A>C	NP_000021.1:n.424-26A>C
NM_000030.3:c.424-26A>C MANE Select	NP_000021.1:n.424-26A>C