Canonical Allele Identifier: CA413308547
Gene: AMER1 HGNC NCBI

Linked Data

dbSNP Id: rs760684276
MyVariant Identifiers: chrX:g.63412089A>T (hg19) chrX:g.64192209A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.64192209A>T , CM000685.2:g.64192209A>T GRCh38
NC_000023.10:g.63412089A>T , CM000685.1:g.63412089A>T GRCh37
NC_000023.9:g.63328814A>T NCBI36
NG_021345.1:g.18536T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000374869.8:c.1078T>A MANE Select ENSP00000364003.4:p.Ser360Thr
ENST00000330258.3:c.1078T>A ENSP00000329117.3:p.Ser360Thr
ENST00000374869.7:c.1078T>A ENSP00000364003.3:p.Ser360Thr
NM_152424.3:c.1078T>A NP_689637.3:p.Ser360Thr
XM_011530858.1:c.1078T>A XP_011529160.1:p.Ser360Thr
NM_152424.4:c.1078T>A MANE Select NP_689637.3:p.Ser360Thr
Search 100 bp 5'
Search 100 bp 3'