Canonical Allele Identifier: CA2664010861

Gene: AGXT

Linked Data

• dbSNP Id: rs2106431585
• gnomAD v4: 2-240877365-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240877365T>C , CM000664.2:g.240877365T>C	GRCh38
NC_000002.11:g.241816782T>C , CM000664.1:g.241816782T>C	GRCh37
NC_000002.10:g.241465455T>C	NCBI36
NG_008005.1:g.13621T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000307503.4:c.847-172T>C MANE Select	ENSP00000302620.3:n.847-172T>C
ENST00000307503.3:c.847-172T>C	ENSP00000302620.3:n.847-172T>C
ENST00000470255.1:n.453T>C
NM_000030.2:c.847-172T>C	NP_000021.1:n.847-172T>C
NM_000030.3:c.847-172T>C MANE Select	NP_000021.1:n.847-172T>C