Canonical Allele Identifier: CA31742116

Gene: OLFML2B

Linked Data

• dbSNP Id: rs185436876
• gnomAD v3: 1-161984849-C-A
• gnomAD v4: 1-161984849-C-A
• MyVariant Identifiers: chr1:g.161954639C>A (hg19) ; chr1:g.161984849C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161984849C>A , CM000663.2:g.161984849C>A	GRCh38
NC_000001.10:g.161954639C>A , CM000663.1:g.161954639C>A	GRCh37
NC_000001.9:g.160221263C>A	NCBI36
NG_052853.1:g.44617G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000294794.8:c.1606G>T MANE Select	ENSP00000294794.3:p.Gly536Cys
ENST00000294794.7:c.1606G>T	ENSP00000294794.3:p.Gly536Cys
ENST00000367938.1:c.55G>T	ENSP00000356915.1:p.Gly19Cys
ENST00000367940.2:c.1609G>T	ENSP00000356917.2:p.Gly537Cys
NM_001297713.1:c.1609G>T	NP_001284642.1:p.Gly537Cys
NM_015441.2:c.1606G>T	NP_056256.1:p.Gly536Cys
XM_005245075.2:c.1612G>T	XP_005245132.1:p.Gly538Cys
XM_011509398.1:c.886G>T	XP_011507700.1:p.Gly296Cys
NM_001347700.1:c.1612G>T	NP_001334629.1:p.Gly538Cys
XM_011509398.2:c.886G>T	XP_011507700.1:p.Gly296Cys
NM_001297713.2:c.1609G>T	NP_001284642.1:p.Gly537Cys
NM_001347700.2:c.1612G>T	NP_001334629.1:p.Gly538Cys
NM_015441.3:c.1606G>T MANE Select	NP_056256.1:p.Gly536Cys