Canonical Allele Identifier: CA517041302
Gene: AMER1 HGNC NCBI

Linked Data

dbSNP Id: rs2147089856
MyVariant Identifiers: chrX:g.63412420A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.64192540A>G , CM000685.2:g.64192540A>G GRCh38
NC_000023.10:g.63412420A>G , CM000685.1:g.63412420A>G GRCh37
NC_000023.9:g.63329145A>G NCBI36
NG_021345.1:g.18205T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000374869.8:c.747T>C MANE Select ENSP00000364003.4:p.Ala249=
ENST00000330258.3:c.747T>C ENSP00000329117.3:p.Ala249=
ENST00000374869.7:c.747T>C ENSP00000364003.3:p.Ala249=
NM_152424.3:c.747T>C NP_689637.3:p.Ala249=
XM_011530858.1:c.747T>C XP_011529160.1:p.Ala249=
NM_152424.4:c.747T>C MANE Select NP_689637.3:p.Ala249=