Canonical Allele Identifier: CA351316578
Gene: AGXT HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.241812439G>T (hg19) chr2:g.240873022G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240873022G>T , CM000664.2:g.240873022G>T GRCh38
NC_000002.11:g.241812439G>T , CM000664.1:g.241812439G>T GRCh37
NC_000002.10:g.241461112G>T NCBI36
NG_008005.1:g.9278G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.568G>T MANE Select ENSP00000302620.3:p.Gly190Trp
ENST00000307503.3:c.568G>T ENSP00000302620.3:p.Gly190Trp
ENST00000472436.1:n.588G>T
ENST00000476698.1:n.305G>T
NM_000030.2:c.568G>T NP_000021.1:p.Gly190Trp
NM_000030.3:c.568G>T MANE Select NP_000021.1:p.Gly190Trp
Search 100 bp 5'
Search 100 bp 3'