Canonical Allele Identifier: CA475200994

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68701299T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68933831T>C , CM000673.2:g.68933831T>C	GRCh38
NC_000011.9:g.68701299T>C , CM000673.1:g.68701299T>C	GRCh37
NC_000011.8:g.68457875T>C	NCBI36
NG_007976.1:g.34981T>C , LRG_250:g.34981T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.1455T>C MANE Select	ENSP00000255078.4:p.Gly485=
ENST00000674955.1:c.*172T>C	ENSP00000502463.1:n.*172T>C
ENST00000675118.1:c.943T>C
ENST00000675205.1:n.183+350T>C
ENST00000675615.1:c.1455T>C	ENSP00000502413.1:p.Gly485=
ENST00000675648.1:n.830T>C
ENST00000675997.1:n.113-633T>C
ENST00000676173.1:n.2200T>C
ENST00000676228.1:c.*778T>C	ENSP00000502375.1:n.*778T>C
ENST00000255078.7:c.1455T>C	ENSP00000255078.3:p.Gly485=
ENST00000537458.5:n.572T>C
ENST00000539064.5:n.1214T>C
ENST00000541229.5:n.150T>C
ENST00000543739.5:n.572T>C
NM_002180.2:c.1455T>C , LRG_250t1:c.1455T>C	NP_002171.2:p.Gly485=
XM_005273974.2:c.444T>C	XP_005274031.1:p.Gly148=
XM_005273975.2:c.327T>C	XP_005274032.1:p.Gly109=
XM_011544994.1:c.222T>C	XP_011543296.1:p.Gly74=
XR_949903.1:n.1557T>C
XM_005273975.3:c.327T>C	XP_005274032.1:p.Gly109=
XM_017017669.2:c.444T>C	XP_016873158.1:p.Gly148=
XM_017017670.2:c.444T>C	XP_016873159.1:p.Gly148=
XM_017017671.2:c.1455T>C	XP_016873160.1:p.Gly485=
XR_949903.3:n.1553T>C
NM_002180.3:c.1455T>C MANE Select	NP_002171.2:p.Gly485=