Canonical Allele Identifier: CA475279016

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68703964C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936496C>G , CM000673.2:g.68936496C>G	GRCh38
NC_000011.9:g.68703964C>G , CM000673.1:g.68703964C>G	GRCh37
NC_000011.8:g.68460540C>G	NCBI36
NG_007976.1:g.37646C>G , LRG_250:g.37646C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.2016C>G MANE Select	ENSP00000255078.4:p.Ser672=
ENST00000674675.1:c.260C>G
ENST00000674878.1:c.260C>G
ENST00000674955.1:c.*733C>G	ENSP00000502463.1:n.*733C>G
ENST00000675118.1:c.1504C>G
ENST00000675389.1:n.291C>G
ENST00000675615.1:c.2016C>G	ENSP00000502413.1:p.Ser672=
ENST00000675648.1:n.1391C>G
ENST00000675916.1:c.260C>G
ENST00000676173.1:n.2761C>G
ENST00000676182.1:c.447C>G
ENST00000676228.1:c.*1339C>G	ENSP00000502375.1:n.*1339C>G
ENST00000255078.7:c.2016C>G	ENSP00000255078.3:p.Ser672=
ENST00000539064.5:n.1775C>G
ENST00000543739.5:n.1009C>G
NM_002180.2:c.2016C>G , LRG_250t1:c.2016C>G	NP_002171.2:p.Ser672=
XM_005273974.2:c.1005C>G	XP_005274031.1:p.Ser335=
XM_005273975.2:c.888C>G	XP_005274032.1:p.Ser296=
XM_011544994.1:c.783C>G	XP_011543296.1:p.Ser261=
XR_949903.1:n.2118C>G
XM_005273975.3:c.888C>G	XP_005274032.1:p.Ser296=
XM_017017669.2:c.1005C>G	XP_016873158.1:p.Ser335=
XM_017017670.2:c.1005C>G	XP_016873159.1:p.Ser335=
XR_949903.3:n.2114C>G
NM_002180.3:c.2016C>G MANE Select	NP_002171.2:p.Ser672=