Canonical Allele Identifier: CA413309839
Gene: AMER1 HGNC NCBI

Linked Data

dbSNP Id: rs2147089913
MyVariant Identifiers: chrX:g.63412443T>G (hg19) chrX:g.64192563T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.64192563T>G , CM000685.2:g.64192563T>G GRCh38
NC_000023.10:g.63412443T>G , CM000685.1:g.63412443T>G GRCh37
NC_000023.9:g.63329168T>G NCBI36
NG_021345.1:g.18182A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000374869.8:c.724A>C MANE Select ENSP00000364003.4:p.Thr242Pro
ENST00000330258.3:c.724A>C ENSP00000329117.3:p.Thr242Pro
ENST00000374869.7:c.724A>C ENSP00000364003.3:p.Thr242Pro
NM_152424.3:c.724A>C NP_689637.3:p.Thr242Pro
XM_011530858.1:c.724A>C XP_011529160.1:p.Thr242Pro
NM_152424.4:c.724A>C MANE Select NP_689637.3:p.Thr242Pro
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