Canonical Allele Identifier: CA517040998
Gene: AMER1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.63412282T>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.64192402T>C , CM000685.2:g.64192402T>C GRCh38
NC_000023.10:g.63412282T>C , CM000685.1:g.63412282T>C GRCh37
NC_000023.9:g.63329007T>C NCBI36
NG_021345.1:g.18343A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000374869.8:c.885A>G MANE Select ENSP00000364003.4:p.Ala295=
ENST00000330258.3:c.885A>G ENSP00000329117.3:p.Ala295=
ENST00000374869.7:c.885A>G ENSP00000364003.3:p.Ala295=
NM_152424.3:c.885A>G NP_689637.3:p.Ala295=
XM_011530858.1:c.885A>G XP_011529160.1:p.Ala295=
NM_152424.4:c.885A>G MANE Select NP_689637.3:p.Ala295=
Search 100 bp 5'
Search 100 bp 3'