Canonical Allele Identifier: CA517041333
Gene: AMER1 HGNC NCBI

Linked Data

dbSNP Id: rs2147089051
MyVariant Identifiers: chrX:g.63412066T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.64192186T>C , CM000685.2:g.64192186T>C GRCh38
NC_000023.10:g.63412066T>C , CM000685.1:g.63412066T>C GRCh37
NC_000023.9:g.63328791T>C NCBI36
NG_021345.1:g.18559A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000374869.8:c.1101A>G MANE Select ENSP00000364003.4:p.Gly367=
ENST00000330258.3:c.1101A>G ENSP00000329117.3:p.Gly367=
ENST00000374869.7:c.1101A>G ENSP00000364003.3:p.Gly367=
NM_152424.3:c.1101A>G NP_689637.3:p.Gly367=
XM_011530858.1:c.1101A>G XP_011529160.1:p.Gly367=
NM_152424.4:c.1101A>G MANE Select NP_689637.3:p.Gly367=
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