Canonical Allele Identifier: CA380181370
Gene: ALX4 HGNC NCBI

Linked Data

gnomAD v4: 11-44265005-G-C
MyVariant Identifiers: chr11:g.44286555G>C (hg19) chr11:g.44265005G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.44265005G>C , CM000673.2:g.44265005G>C GRCh38
NC_000011.9:g.44286555G>C , CM000673.1:g.44286555G>C GRCh37
NC_000011.8:g.44243131G>C NCBI36
NG_015809.1:g.50162C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000652299.1:c.1085C>G MANE Select ENSP00000498217.1:p.Thr362Arg
ENST00000329255.3:c.1085C>G ENSP00000332744.3:p.Thr362Arg
NM_021926.3:c.1085C>G NP_068745.2:p.Thr362Arg
XM_011520265.1:c.563C>G XP_011518567.1:p.Thr188Arg
XM_011520266.1:c.563C>G XP_011518568.1:p.Thr188Arg
NM_021926.4:c.1085C>G MANE Select NP_068745.2:p.Thr362Arg
Search 100 bp 5'
Search 100 bp 3'