Canonical Allele Identifier: CA589466880
Gene: BARX1 HGNC NCBI

Linked Data

dbSNP Id: rs1462523263
gnomAD v2: 9-96716435-G-A
gnomAD v3: 9-93954153-G-A
gnomAD v4: 9-93954153-G-A
MyVariant Identifiers: chr9:g.96716435G>A (hg19) chr9:g.93954153G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.93954153G>A , CM000671.2:g.93954153G>A GRCh38
NC_000009.11:g.96716435G>A , CM000671.1:g.96716435G>A GRCh37
NC_000009.10:g.95756256G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000253968.11:c.223+771C>T MANE Select ENSP00000253968.5:n.223+771C>T
ENST00000253968.10:c.223+771C>T ENSP00000253968.5:n.223+771C>T
NM_021570.3:c.223+771C>T NP_067545.3:n.223+771C>T
NM_021570.4:c.223+771C>T MANE Select NP_067545.3:n.223+771C>T
Search 100 bp 5'
Search 100 bp 3'