Canonical Allele Identifier: CA413309600
Gene: AMER1 HGNC NCBI

Linked Data

dbSNP Id: rs1404713868
gnomAD v2: X-63412391-T-A
gnomAD v4: X-64192511-T-A
MyVariant Identifiers: chrX:g.63412391T>A (hg19) chrX:g.64192511T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.64192511T>A , CM000685.2:g.64192511T>A GRCh38
NC_000023.10:g.63412391T>A , CM000685.1:g.63412391T>A GRCh37
NC_000023.9:g.63329116T>A NCBI36
NG_021345.1:g.18234A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000374869.8:c.776A>T MANE Select ENSP00000364003.4:p.Glu259Val
ENST00000330258.3:c.776A>T ENSP00000329117.3:p.Glu259Val
ENST00000374869.7:c.776A>T ENSP00000364003.3:p.Glu259Val
NM_152424.3:c.776A>T NP_689637.3:p.Glu259Val
XM_011530858.1:c.776A>T XP_011529160.1:p.Glu259Val
NM_152424.4:c.776A>T MANE Select NP_689637.3:p.Glu259Val
Search 100 bp 5'
Search 100 bp 3'