Canonical Allele Identifier: CA196446614
Gene: BARX1 HGNC NCBI

Linked Data

dbSNP Id: rs184234212
gnomAD v2: 9-96715645-C-A
gnomAD v3: 9-93953363-C-A
gnomAD v4: 9-93953363-C-A
MyVariant Identifiers: chr9:g.96715645C>A (hg19) chr9:g.93953363C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.93953363C>A , CM000671.2:g.93953363C>A GRCh38
NC_000009.11:g.96715645C>A , CM000671.1:g.96715645C>A GRCh37
NC_000009.10:g.95755466C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000253968.11:c.224-176G>T MANE Select ENSP00000253968.5:n.224-176G>T
ENST00000253968.10:c.224-176G>T ENSP00000253968.5:n.224-176G>T
ENST00000401724.1:c.-415G>T ENSP00000385613.1:n.-415G>T
NM_021570.3:c.224-176G>T NP_067545.3:n.224-176G>T
NM_021570.4:c.224-176G>T MANE Select NP_067545.3:n.224-176G>T
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