Canonical Allele Identifier: CA2209422
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs375318394

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.1110C>T MANE Select ENSP00000302620.3:p.Arg370=
ENST00000307503.3:c.1110C>T ENSP00000302620.3:p.Arg370=
ENST00000470255.1:n.888C>T
NM_000030.2:c.1110C>T NP_000021.1:p.Arg370=
NM_000030.3:c.1110C>T MANE Select NP_000021.1:p.Arg370=