Canonical Allele Identifier: CA10432419
Gene: AMER1 HGNC NCBI

Linked Data

dbSNP Id: rs747197554
ExAC: X:63412313 T / C
gnomAD v2: X-63412313-T-C
gnomAD v3: X-64192433-T-C
gnomAD v4: X-64192433-T-C
MyVariant Identifiers: chrX:g.63412313T>C (hg19) chrX:g.64192433T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.64192433T>C , CM000685.2:g.64192433T>C GRCh38
NC_000023.10:g.63412313T>C , CM000685.1:g.63412313T>C GRCh37
NC_000023.9:g.63329038T>C NCBI36
NG_021345.1:g.18312A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000374869.8:c.854A>G MANE Select ENSP00000364003.4:p.His285Arg
ENST00000330258.3:c.854A>G ENSP00000329117.3:p.His285Arg
ENST00000374869.7:c.854A>G ENSP00000364003.3:p.His285Arg
NM_152424.3:c.854A>G NP_689637.3:p.His285Arg
XM_011530858.1:c.854A>G XP_011529160.1:p.His285Arg
NM_152424.4:c.854A>G MANE Select NP_689637.3:p.His285Arg
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