Canonical Allele Identifier: CA221487557
Gene: ALX4 HGNC NCBI

Linked Data

dbSNP Id: rs1039616189
gnomAD v2: 11-44286560-G-A
gnomAD v3: 11-44265010-G-A
gnomAD v4: 11-44265010-G-A
MyVariant Identifiers: chr11:g.44286560G>A (hg19) chr11:g.44265010G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.44265010G>A , CM000673.2:g.44265010G>A GRCh38
NC_000011.9:g.44286560G>A , CM000673.1:g.44286560G>A GRCh37
NC_000011.8:g.44243136G>A NCBI36
NG_015809.1:g.50157C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000652299.1:c.1080C>T MANE Select ENSP00000498217.1:p.Gly360=
ENST00000329255.3:c.1080C>T ENSP00000332744.3:p.Gly360=
NM_021926.3:c.1080C>T NP_068745.2:p.Gly360=
XM_011520265.1:c.558C>T XP_011518567.1:p.Gly186=
XM_011520266.1:c.558C>T XP_011518568.1:p.Gly186=
NM_021926.4:c.1080C>T MANE Select NP_068745.2:p.Gly360=
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