Canonical Allele Identifier: CA357827327

Gene: SGMS2 CYP2U1-AS1

Linked Data

• MyVariant Identifiers: chr4:g.108829777G>C (hg19) ; chr4:g.107908621G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.107908621G>C , CM000666.2:g.107908621G>C	GRCh38
NC_000004.11:g.108829777G>C , CM000666.1:g.108829777G>C	GRCh37
NC_000004.10:g.109049226G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690982.1:c.784G>C (SGMS2) MANE Select	ENSP00000508566.1:p.Gly262Arg
ENST00000359079.8:c.784G>C (SGMS2)	ENSP00000351981.4:p.Gly262Arg
ENST00000394684.8:c.784G>C (SGMS2)	ENSP00000378176.4:p.Gly262Arg
ENST00000394686.3:c.784G>C (SGMS2)	ENSP00000378178.3:p.Gly262Arg
ENST00000503862.5:c.265G>C (SGMS2)	ENSP00000428176.1:p.Gly89Arg
NM_001136257.1:c.784G>C (SGMS2)	NP_001129729.1:p.Gly262Arg
NM_001136258.1:c.784G>C (SGMS2)	NP_001129730.1:p.Gly262Arg
NM_152621.5:c.784G>C (SGMS2)	NP_689834.1:p.Gly262Arg
NR_125929.1:n.150-14984C>G (CYP2U1-AS1)
XM_006714121.1:c.784G>C (SGMS2)	XP_006714184.1:p.Gly262Arg
XM_011531698.1:c.784G>C (SGMS2)	XP_011530000.1:p.Gly262Arg
XM_011531699.1:c.784G>C (SGMS2)	XP_011530001.1:p.Gly262Arg
XM_011531700.1:c.784G>C (SGMS2)	XP_011530002.1:p.Gly262Arg
XM_011531701.1:c.784G>C (SGMS2)	XP_011530003.1:p.Gly262Arg
XM_011531702.1:c.784G>C (SGMS2)	XP_011530004.1:p.Gly262Arg
XM_011531698.2:c.784G>C (SGMS2)	XP_011530000.1:p.Gly262Arg
XM_011531699.2:c.784G>C (SGMS2)	XP_011530001.1:p.Gly262Arg
XM_011531700.2:c.784G>C (SGMS2)	XP_011530002.1:p.Gly262Arg
XM_011531701.2:c.784G>C (SGMS2)	XP_011530003.1:p.Gly262Arg
XM_011531702.2:c.784G>C (SGMS2)	XP_011530004.1:p.Gly262Arg
XM_017007839.1:c.784G>C (SGMS2)	XP_016863328.1:p.Gly262Arg
XM_017007841.1:c.728-1729G>C (SGMS2)	XP_016863330.1:n.728-1729G>C
XR_001741783.1:n.2084C>G
XR_001741784.1:n.2459C>G
NM_001136257.2:c.784G>C (SGMS2)	NP_001129729.1:p.Gly262Arg
NM_001136258.2:c.784G>C (SGMS2)	NP_001129730.1:p.Gly262Arg
NM_001375905.1:c.784G>C (SGMS2) MANE Select	NP_001362834.1:p.Gly262Arg
NM_001375906.1:c.784G>C (SGMS2)	NP_001362835.1:p.Gly262Arg
NM_001375907.1:c.784G>C (SGMS2)	NP_001362836.1:p.Gly262Arg
NM_001375908.1:c.784G>C (SGMS2)	NP_001362837.1:p.Gly262Arg
NM_001375910.1:c.728-1729G>C (SGMS2)	NP_001362839.1:n.728-1729G>C
NM_001375911.1:c.265G>C (SGMS2)	NP_001362840.1:p.Gly89Arg
NM_152621.6:c.784G>C (SGMS2)	NP_689834.1:p.Gly262Arg