Canonical Allele Identifier: CA381653677

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68704398A>C (hg19) ; chr11:g.68936930A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936930A>C , CM000673.2:g.68936930A>C	GRCh38
NC_000011.9:g.68704398A>C , CM000673.1:g.68704398A>C	GRCh37
NC_000011.8:g.68460974A>C	NCBI36
NG_007976.1:g.38080A>C , LRG_250:g.38080A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000255078.8:c.2450A>C MANE Select	ENSP00000255078.4:p.Gln817Pro
ENST00000674675.1:c.595A>C
ENST00000674878.1:c.555A>C
ENST00000675118.1:c.1938A>C
ENST00000675389.1:n.725A>C
ENST00000675615.1:c.2450A>C	ENSP00000502413.1:p.Gln817Pro
ENST00000675648.1:n.1825A>C
ENST00000675916.1:c.694A>C
ENST00000676173.1:n.3195A>C
ENST00000676182.1:c.881A>C
ENST00000676228.1:c.*1773A>C	ENSP00000502375.1:n.*1773A>C
ENST00000255078.7:c.2450A>C	ENSP00000255078.3:p.Gln817Pro
ENST00000539064.5:n.2209A>C
ENST00000543739.5:n.1443A>C
NM_002180.2:c.2450A>C , LRG_250t1:c.2450A>C	NP_002171.2:p.Gln817Pro
XM_005273974.2:c.1439A>C	XP_005274031.1:p.Gln480Pro
XM_005273975.2:c.1322A>C	XP_005274032.1:p.Gln441Pro
XM_011544994.1:c.1217A>C	XP_011543296.1:p.Gln406Pro
XR_949903.1:n.2552A>C
XM_005273975.3:c.1322A>C	XP_005274032.1:p.Gln441Pro
XM_017017669.2:c.1439A>C	XP_016873158.1:p.Gln480Pro
XM_017017670.2:c.1439A>C	XP_016873159.1:p.Gln480Pro
XR_949903.3:n.2548A>C
NM_002180.3:c.2450A>C MANE Select	NP_002171.2:p.Gln817Pro