Canonical Allele Identifier: CA351319755
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs1231173243
gnomAD v2: 2-241818152-G-A
gnomAD v4: 2-240878735-G-A
MyVariant Identifiers: chr2:g.241818152G>A (hg19) chr2:g.240878735G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878735G>A , CM000664.2:g.240878735G>A GRCh38
NC_000002.11:g.241818152G>A , CM000664.1:g.241818152G>A GRCh37
NC_000002.10:g.241466825G>A NCBI36
NG_008005.1:g.14991G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.1093G>A MANE Select ENSP00000302620.3:p.Gly365Ser
ENST00000307503.3:c.1093G>A ENSP00000302620.3:p.Gly365Ser
ENST00000470255.1:n.871G>A
NM_000030.2:c.1093G>A NP_000021.1:p.Gly365Ser
NM_000030.3:c.1093G>A MANE Select NP_000021.1:p.Gly365Ser
Search 100 bp 5'
Search 100 bp 3'