Canonical Allele Identifier: CA381652047

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68703881G>C (hg19) ; chr11:g.68936413G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936413G>C , CM000673.2:g.68936413G>C	GRCh38
NC_000011.9:g.68703881G>C , CM000673.1:g.68703881G>C	GRCh37
NC_000011.8:g.68460457G>C	NCBI36
NG_007976.1:g.37563G>C , LRG_250:g.37563G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000255078.8:c.1933G>C MANE Select	ENSP00000255078.4:p.Asp645His
ENST00000674675.1:c.177G>C
ENST00000674878.1:c.177G>C
ENST00000674955.1:c.*650G>C	ENSP00000502463.1:n.*650G>C
ENST00000675118.1:c.1421G>C
ENST00000675389.1:n.208G>C
ENST00000675615.1:c.1933G>C	ENSP00000502413.1:p.Asp645His
ENST00000675648.1:n.1308G>C
ENST00000675916.1:c.177G>C
ENST00000676173.1:n.2678G>C
ENST00000676182.1:c.364G>C
ENST00000676228.1:c.*1256G>C	ENSP00000502375.1:n.*1256G>C
ENST00000255078.7:c.1933G>C	ENSP00000255078.3:p.Asp645His
ENST00000539064.5:n.1692G>C
ENST00000543739.5:n.926G>C
ENST00000545475.1:n.529G>C
NM_002180.2:c.1933G>C , LRG_250t1:c.1933G>C	NP_002171.2:p.Asp645His
XM_005273974.2:c.922G>C	XP_005274031.1:p.Asp308His
XM_005273975.2:c.805G>C	XP_005274032.1:p.Asp269His
XM_011544994.1:c.700G>C	XP_011543296.1:p.Asp234His
XR_949903.1:n.2035G>C
XM_005273975.3:c.805G>C	XP_005274032.1:p.Asp269His
XM_017017669.2:c.922G>C	XP_016873158.1:p.Asp308His
XM_017017670.2:c.922G>C	XP_016873159.1:p.Asp308His
XR_949903.3:n.2031G>C
NM_002180.3:c.1933G>C MANE Select	NP_002171.2:p.Asp645His