Canonical Allele Identifier: CA812012637
Gene: ITGA1 HGNC NCBI

Linked Data

dbSNP Id: rs1482393523
gnomAD v3: 5-52899212-G-C
gnomAD v4: 5-52899212-G-C
MyVariant Identifiers: chr5:g.52195042G>C (hg19) chr5:g.52899212G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.52899212G>C , CM000667.2:g.52899212G>C GRCh38
NC_000005.9:g.52195042G>C , CM000667.1:g.52195042G>C GRCh37
NC_000005.8:g.52230799G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000282588.7:c.1309+829G>C MANE Select ENSP00000282588.5:n.1309+829G>C
ENST00000650673.1:c.*471+829G>C ENSP00000498529.1:n.*471+829G>C
ENST00000282588.6:c.1309+829G>C ENSP00000282588.5:n.1309+829G>C
NM_181501.1:c.1309+829G>C NP_852478.1:n.1309+829G>C
NM_181501.2:c.1309+829G>C MANE Select NP_852478.1:n.1309+829G>C
Search 100 bp 5'
Search 100 bp 3'