Canonical Allele Identifier: CA221487556
Gene: ALX4 HGNC NCBI

Linked Data

dbSNP Id: rs772445432
gnomAD v4: 11-44265008-T-C
MyVariant Identifiers: chr11:g.44286558T>C (hg19) chr11:g.44265008T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.44265008T>C , CM000673.2:g.44265008T>C GRCh38
NC_000011.9:g.44286558T>C , CM000673.1:g.44286558T>C GRCh37
NC_000011.8:g.44243134T>C NCBI36
NG_015809.1:g.50159A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000652299.1:c.1082A>G MANE Select ENSP00000498217.1:p.Gln361Arg
ENST00000329255.3:c.1082A>G ENSP00000332744.3:p.Gln361Arg
NM_021926.3:c.1082A>G NP_068745.2:p.Gln361Arg
XM_011520265.1:c.560A>G XP_011518567.1:p.Gln187Arg
XM_011520266.1:c.560A>G XP_011518568.1:p.Gln187Arg
NM_021926.4:c.1082A>G MANE Select NP_068745.2:p.Gln361Arg
Search 100 bp 5'
Search 100 bp 3'