Canonical Allele Identifier: CA432026969
Gene: AGXT HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.241818146C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878729C>T , CM000664.2:g.240878729C>T GRCh38
NC_000002.11:g.241818146C>T , CM000664.1:g.241818146C>T GRCh37
NC_000002.10:g.241466819C>T NCBI36
NG_008005.1:g.14985C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.1087C>T MANE Select ENSP00000302620.3:p.Leu363=
ENST00000307503.3:c.1087C>T ENSP00000302620.3:p.Leu363=
ENST00000470255.1:n.865C>T
NM_000030.2:c.1087C>T NP_000021.1:p.Leu363=
NM_000030.3:c.1087C>T MANE Select NP_000021.1:p.Leu363=
Search 100 bp 5'
Search 100 bp 3'