Canonical Allele Identifier: CA432027048
Gene: AGXT HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.241818169C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878752C>G , CM000664.2:g.240878752C>G GRCh38
NC_000002.11:g.241818169C>G , CM000664.1:g.241818169C>G GRCh37
NC_000002.10:g.241466842C>G NCBI36
NG_008005.1:g.15008C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.1110C>G MANE Select ENSP00000302620.3:p.Arg370=
ENST00000307503.3:c.1110C>G ENSP00000302620.3:p.Arg370=
ENST00000470255.1:n.888C>G
NM_000030.2:c.1110C>G NP_000021.1:p.Arg370=
NM_000030.3:c.1110C>G MANE Select NP_000021.1:p.Arg370=
Search 100 bp 5'
Search 100 bp 3'