Canonical Allele Identifier: CA413309178
Gene: AMER1 HGNC NCBI

Linked Data

dbSNP Id: rs1435543004

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.64192418C>A , CM000685.2:g.64192418C>A GRCh38
NC_000023.10:g.63412298C>A , CM000685.1:g.63412298C>A GRCh37
NC_000023.9:g.63329023C>A NCBI36
NG_021345.1:g.18327G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000374869.8:c.869G>T MANE Select ENSP00000364003.4:p.Gly290Val
ENST00000330258.3:c.869G>T ENSP00000329117.3:p.Gly290Val
ENST00000374869.7:c.869G>T ENSP00000364003.3:p.Gly290Val
NM_152424.3:c.869G>T NP_689637.3:p.Gly290Val
XM_011530858.1:c.869G>T XP_011529160.1:p.Gly290Val
NM_152424.4:c.869G>T MANE Select NP_689637.3:p.Gly290Val