Canonical Allele Identifier: CA766958659
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs1251379720
gnomAD v3: 2-240878211-A-G
gnomAD v4: 2-240878211-A-G
MyVariant Identifiers: chr2:g.241817628A>G (hg19) chr2:g.240878211A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878211A>G , CM000664.2:g.240878211A>G GRCh38
NC_000002.11:g.241817628A>G , CM000664.1:g.241817628A>G GRCh37
NC_000002.10:g.241466301A>G NCBI36
NG_008005.1:g.14467A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.1071+61A>G MANE Select ENSP00000302620.3:n.1071+61A>G
ENST00000307503.3:c.1071+61A>G ENSP00000302620.3:n.1071+61A>G
ENST00000470255.1:n.849+61A>G
NM_000030.2:c.1071+61A>G NP_000021.1:n.1071+61A>G
NM_000030.3:c.1071+61A>G MANE Select NP_000021.1:n.1071+61A>G
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