Canonical Allele Identifier: CA9181190

Gene: OLFM2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.9854147A>G , CM000681.2:g.9854147A>G	GRCh38
NC_000019.9:g.9964823A>G , CM000681.1:g.9964823A>G	GRCh37
NC_000019.8:g.9825823A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264833.9:c.*39T>C MANE Select	ENSP00000264833.3:n.*39T>C
ENST00000593091.2:c.*39T>C	ENSP00000465809.2:n.*39T>C
ENST00000264833.8:c.*39T>C	ENSP00000264833.3:n.*39T>C
ENST00000590841.5:c.*39T>C	ENSP00000464877.1:n.*39T>C
NM_001304347.1:c.*39T>C	NP_001291276.1:n.*39T>C
NM_001304348.1:c.*39T>C	NP_001291277.1:n.*39T>C
NM_058164.3:c.*39T>C	NP_477512.1:n.*39T>C
NM_001304347.2:c.*39T>C	NP_001291276.1:n.*39T>C
NM_001304348.2:c.*39T>C	NP_001291277.1:n.*39T>C
NM_058164.4:c.*39T>C MANE Select	NP_477512.1:n.*39T>C