Canonical Allele Identifier: CA2958910988

Gene: OSMR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.38904283G>T , CM000667.2:g.38904283G>T	GRCh38
NC_000005.9:g.38904385G>T , CM000667.1:g.38904385G>T	GRCh37
NC_000005.8:g.38940142G>T	NCBI36
NG_016236.1:g.63426G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_003999.3:c.1135-70G>T MANE Select	NP_003990.1:n.1135-70G>T
ENST00000274276.8:c.1135-70G>T MANE Select	ENSP00000274276.3:n.1135-70G>T
NM_001323505.1:c.1135-70G>T	NP_001310434.1:n.1135-70G>T
NM_001323505.2:c.1135-70G>T	NP_001310434.1:n.1135-70G>T
NM_001323506.1:c.1135-67G>T	NP_001310435.1:n.1135-67G>T
NM_001323506.2:c.1135-67G>T	NP_001310435.1:n.1135-67G>T
NM_001323507.1:c.1135-70G>T	NP_001310436.1:n.1135-70G>T
NM_001323507.2:c.1135-70G>T	NP_001310436.1:n.1135-70G>T
NM_003999.2:c.1135-70G>T	NP_003990.1:n.1135-70G>T
ENST00000274276.7:c.1135-70G>T	ENSP00000274276.3:n.1135-70G>T
XM_005248384.1:c.1135-67G>T	XP_005248441.1:n.1135-67G>T
XM_005248385.1:c.1135-67G>T	XP_005248442.1:n.1135-67G>T
XM_005248386.2:c.1135-67G>T	XP_005248443.1:n.1135-67G>T
XM_005248387.2:c.1135-70G>T	XP_005248444.1:n.1135-70G>T
XM_011514161.1:c.1135-67G>T	XP_011512463.1:n.1135-67G>T
XM_011514161.2:c.1135-67G>T	XP_011512463.1:n.1135-67G>T
XM_017010019.1:c.1135-70G>T	XP_016865508.1:n.1135-70G>T
XR_925661.1:n.1524-67G>T