Canonical Allele Identifier: CA351318189
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875170G>C , CM000664.2:g.240875170G>C GRCh38
NC_000002.11:g.241814587G>C , CM000664.1:g.241814587G>C GRCh37
NC_000002.10:g.241463260G>C NCBI36
NG_008005.1:g.11426G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.742G>C MANE Select ENSP00000302620.3:p.Ala248Pro
ENST00000307503.3:c.742G>C ENSP00000302620.3:p.Ala248Pro
ENST00000476698.1:n.394G>C
NM_000030.2:c.742G>C NP_000021.1:p.Ala248Pro
NM_000030.3:c.742G>C MANE Select NP_000021.1:p.Ala248Pro