Canonical Allele Identifier: CA413308882
Gene: AMER1 HGNC NCBI

Linked Data

dbSNP Id: rs1930267473

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.64192350A>T , CM000685.2:g.64192350A>T GRCh38
NC_000023.10:g.63412230A>T , CM000685.1:g.63412230A>T GRCh37
NC_000023.9:g.63328955A>T NCBI36
NG_021345.1:g.18395T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000374869.8:c.937T>A MANE Select ENSP00000364003.4:p.Phe313Ile
ENST00000330258.3:c.937T>A ENSP00000329117.3:p.Phe313Ile
ENST00000374869.7:c.937T>A ENSP00000364003.3:p.Phe313Ile
NM_152424.3:c.937T>A NP_689637.3:p.Phe313Ile
XM_011530858.1:c.937T>A XP_011529160.1:p.Phe313Ile
NM_152424.4:c.937T>A MANE Select NP_689637.3:p.Phe313Ile