Canonical Allele Identifier: CA473833880
Gene: ALX4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.44296943C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.44275393C>T , CM000673.2:g.44275393C>T GRCh38
NC_000011.9:g.44296943C>T , CM000673.1:g.44296943C>T GRCh37
NC_000011.8:g.44253519C>T NCBI36
NG_015809.1:g.39774G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000652299.1:c.732G>A MANE Select ENSP00000498217.1:p.Arg244=
ENST00000329255.3:c.732G>A ENSP00000332744.3:p.Arg244=
NM_021926.3:c.732G>A NP_068745.2:p.Arg244=
XM_011520264.1:c.732G>A XP_011518566.1:p.Arg244=
XM_011520265.1:c.210G>A XP_011518567.1:p.Arg70=
XM_011520266.1:c.210G>A XP_011518568.1:p.Arg70=
NM_021926.4:c.732G>A MANE Select NP_068745.2:p.Arg244=
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Search 100 bp 3'