Canonical Allele Identifier: CA381643453

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68676022A>C (hg19) ; chr11:g.68908554A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68908554A>C , CM000673.2:g.68908554A>C	GRCh38
NC_000011.9:g.68676022A>C , CM000673.1:g.68676022A>C	GRCh37
NC_000011.8:g.68432598A>C	NCBI36
NG_007976.1:g.9704A>C , LRG_250:g.9704A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.470A>C MANE Select	ENSP00000255078.4:p.Lys157Thr
ENST00000539224.2:c.433A>C
ENST00000674583.1:c.433A>C
ENST00000674597.1:c.281A>C
ENST00000674955.1:c.470A>C	ENSP00000502463.1:p.Lys157Thr
ENST00000675142.1:n.433A>C
ENST00000675469.1:c.346A>C
ENST00000675615.1:c.470A>C	ENSP00000502413.1:p.Lys157Thr
ENST00000675674.1:n.433A>C
ENST00000675683.1:c.21A>C
ENST00000675873.1:c.433A>C
ENST00000676173.1:n.514A>C
ENST00000676228.1:c.449+217A>C	ENSP00000502375.1:n.449+217A>C
ENST00000255078.7:c.470A>C	ENSP00000255078.3:p.Lys157Thr
ENST00000539224.1:c.449+217A>C	ENSP00000440465.1:n.449+217A>C
ENST00000544541.1:c.*210A>C	ENSP00000443343.1:n.*210A>C
NM_002180.2:c.470A>C , LRG_250t1:c.470A>C	NP_002171.2:p.Lys157Thr
XM_005273974.2:c.-542A>C	XP_005274031.1:n.-542A>C
XM_005273976.1:c.470A>C	XP_005274033.1:p.Lys157Thr
XR_247198.1:n.572A>C
XR_949903.1:n.572A>C
XM_005273976.2:c.470A>C	XP_005274033.1:p.Lys157Thr
XM_017017669.2:c.-465+217A>C	XP_016873158.1:n.-465+217A>C
XM_017017671.2:c.470A>C	XP_016873160.1:p.Lys157Thr
XR_949903.3:n.568A>C
NM_002180.3:c.470A>C MANE Select	NP_002171.2:p.Lys157Thr