Canonical Allele Identifier: CA2009739
Gene: ITGA4 HGNC NCBI

Linked Data

dbSNP Id: rs1143674

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.181509807A>G , CM000664.2:g.181509807A>G GRCh38
NC_000002.11:g.182374534A>G , CM000664.1:g.182374534A>G GRCh37
NC_000002.10:g.182082779A>G NCBI36
NG_050623.1:g.57916A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000397033.7:c.1845A>G MANE Select ENSP00000380227.2:p.Thr615=
ENST00000397033.6:c.1845A>G ENSP00000380227.2:p.Thr615=
ENST00000476824.1:n.356A>G
ENST00000490435.5:n.647A>G
NM_000885.4:c.1845A>G NP_000876.3:p.Thr615=
NM_000885.5:c.1845A>G NP_000876.3:p.Thr615=
NM_000885.6:c.1845A>G MANE Select NP_000876.3:p.Thr615=