Canonical Allele Identifier: CA1044064456
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs1023809553

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868559G>C , CM000664.2:g.240868559G>C GRCh38
NC_000002.11:g.241807976G>C , CM000664.1:g.241807976G>C GRCh37
NC_000002.10:g.241456649G>C NCBI36
NG_008005.1:g.4815G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.3:c.-307G>C ENSP00000302620.3:n.-307G>C
XR_924060.1:n.405+1674C>G