Canonical Allele Identifier: CA860706073

Gene: OBP2B

Linked Data

• dbSNP Id: rs139911703
• gnomAD v3: 9-133206500-G-T
• gnomAD v4: 9-133206500-G-T
• MyVariant Identifiers: chr9:g.133206500G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133206500G>T , CM000671.2:g.133206500G>T	GRCh38
NC_000009.10:g.135071708G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000372034.8:c.389-84C>A MANE Select	ENSP00000361104.3:n.389-84C>A
ENST00000372032.3:c.389-19C>A	ENSP00000361102.3:n.389-19C>A
ENST00000372034.7:c.389-84C>A	ENSP00000361104.3:n.389-84C>A
ENST00000461961.2:n.297-84C>A
ENST00000473737.5:c.495-84C>A	ENSP00000434927.1:n.495-84C>A
ENST00000618116.4:c.389-84C>A	ENSP00000484615.1:n.389-84C>A
NM_001288987.1:c.389-84C>A	NP_001275916.1:n.389-84C>A
NM_014581.3:c.389-84C>A	NP_055396.1:n.389-84C>A
NR_110242.1:n.546-84C>A
NR_110243.1:n.306-84C>A
XM_006717086.2:c.290-84C>A	XP_006717149.1:n.290-84C>A
XM_011518605.1:c.545-84C>A	XP_011516907.1:n.545-84C>A
XM_011518606.1:c.545-84C>A	XP_011516908.1:n.545-84C>A
XM_011518607.1:c.545-84C>A	XP_011516909.1:n.545-84C>A
XR_929784.1:n.1690-84C>A
XM_006717086.3:c.290-84C>A	XP_006717149.1:n.290-84C>A
XM_017014654.1:c.545-84C>A	XP_016870143.1:n.545-84C>A
XM_024447527.1:c.545-84C>A	XP_024303295.1:n.545-84C>A
NM_001288987.2:c.389-84C>A	NP_001275916.1:n.389-84C>A
NM_014581.4:c.389-84C>A MANE Select	NP_055396.1:n.389-84C>A
NR_110242.2:n.546-84C>A
NR_110243.2:n.306-84C>A