Canonical Allele Identifier: CA474035693
Gene: ALX4 HGNC NCBI

Linked Data

dbSNP Id: rs1565001606
MyVariant Identifiers: chr11:g.44297078G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.44275528G>T , CM000673.2:g.44275528G>T GRCh38
NC_000011.9:g.44297078G>T , CM000673.1:g.44297078G>T GRCh37
NC_000011.8:g.44253654G>T NCBI36
NG_015809.1:g.39639C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000652299.1:c.597C>A MANE Select ENSP00000498217.1:p.Pro199=
ENST00000329255.3:c.597C>A ENSP00000332744.3:p.Pro199=
NM_021926.3:c.597C>A NP_068745.2:p.Pro199=
XM_011520264.1:c.597C>A XP_011518566.1:p.Pro199=
XM_011520265.1:c.75C>A XP_011518567.1:p.Pro25=
XM_011520266.1:c.75C>A XP_011518568.1:p.Pro25=
NM_021926.4:c.597C>A MANE Select NP_068745.2:p.Pro199=