Canonical Allele Identifier: CA413308151
Gene: AMER1 HGNC NCBI

Linked Data

dbSNP Id: rs2147088767
MyVariant Identifiers: chrX:g.63411921A>C (hg19) chrX:g.64192041A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.64192041A>C , CM000685.2:g.64192041A>C GRCh38
NC_000023.10:g.63411921A>C , CM000685.1:g.63411921A>C GRCh37
NC_000023.9:g.63328646A>C NCBI36
NG_021345.1:g.18704T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000374869.8:c.1246T>G MANE Select ENSP00000364003.4:p.Tyr416Asp
ENST00000330258.3:c.1246T>G ENSP00000329117.3:p.Tyr416Asp
ENST00000374869.7:c.1246T>G ENSP00000364003.3:p.Tyr416Asp
NM_152424.3:c.1246T>G NP_689637.3:p.Tyr416Asp
XM_011530858.1:c.1246T>G XP_011529160.1:p.Tyr416Asp
NM_152424.4:c.1246T>G MANE Select NP_689637.3:p.Tyr416Asp
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