Canonical Allele Identifier: CA766965180
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs1255133082
MyVariant Identifiers: chr2:g.241814832G>T (hg19) chr2:g.240875415G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875415G>T , CM000664.2:g.240875415G>T GRCh38
NC_000002.11:g.241814832G>T , CM000664.1:g.241814832G>T GRCh37
NC_000002.10:g.241463505G>T NCBI36
NG_008005.1:g.11671G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.776+211G>T MANE Select ENSP00000302620.3:n.776+211G>T
ENST00000307503.3:c.776+211G>T ENSP00000302620.3:n.776+211G>T
ENST00000476698.1:n.428+211G>T
NM_000030.2:c.776+211G>T NP_000021.1:n.776+211G>T
NM_000030.3:c.776+211G>T MANE Select NP_000021.1:n.776+211G>T
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