Canonical Allele Identifier: CA474035367
Gene: ALX4 HGNC NCBI

Linked Data

dbSNP Id: rs1252812882
gnomAD v2: 11-44286656-C-A
gnomAD v3: 11-44265106-C-A
gnomAD v4: 11-44265106-C-A
MyVariant Identifiers: chr11:g.44286656C>A (hg19) chr11:g.44265106C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.44265106C>A , CM000673.2:g.44265106C>A GRCh38
NC_000011.9:g.44286656C>A , CM000673.1:g.44286656C>A GRCh37
NC_000011.8:g.44243232C>A NCBI36
NG_015809.1:g.50061G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000652299.1:c.984G>T MANE Select ENSP00000498217.1:p.Val328=
ENST00000329255.3:c.984G>T ENSP00000332744.3:p.Val328=
NM_021926.3:c.984G>T NP_068745.2:p.Val328=
XM_011520265.1:c.462G>T XP_011518567.1:p.Val154=
XM_011520266.1:c.462G>T XP_011518568.1:p.Val154=
NM_021926.4:c.984G>T MANE Select NP_068745.2:p.Val328=
Search 100 bp 5'
Search 100 bp 3'