Canonical Allele Identifier: CA2792557225

Gene: IGHMBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68914813C>G , CM000673.2:g.68914813C>G	GRCh38
NC_000011.9:g.68682281C>G , CM000673.1:g.68682281C>G	GRCh37
NC_000011.8:g.68438857C>G	NCBI36
NG_007976.1:g.15963C>G , LRG_250:g.15963C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.712-10C>G MANE Select	ENSP00000255078.4:n.712-10C>G
ENST00000539224.2:c.841-10C>G
ENST00000674955.1:c.712-10C>G	ENSP00000502463.1:n.712-10C>G
ENST00000675118.1:c.59-10C>G
ENST00000675615.1:c.712-10C>G	ENSP00000502413.1:n.712-10C>G
ENST00000675683.1:c.99-10C>G
ENST00000676173.1:n.756-10C>G
ENST00000676228.1:c.*35-10C>G	ENSP00000502375.1:n.*35-10C>G
ENST00000676239.1:n.26-10C>G
ENST00000255078.7:c.712-10C>G	ENSP00000255078.3:n.712-10C>G
ENST00000539224.1:c.*35-10C>G	ENSP00000440465.1:n.*35-10C>G
NM_002180.2:c.712-10C>G , LRG_250t1:c.712-10C>G	NP_002171.2:n.712-10C>G
XM_005273974.2:c.-300-10C>G	XP_005274031.1:n.-300-10C>G
XM_005273976.1:c.712-10C>G	XP_005274033.1:n.712-10C>G
XR_247198.1:n.814-10C>G
XR_949903.1:n.814-10C>G
XM_005273976.2:c.712-10C>G	XP_005274033.1:n.712-10C>G
XM_017017669.2:c.-300-10C>G	XP_016873158.1:n.-300-10C>G
XM_017017670.2:c.-300-10C>G	XP_016873159.1:n.-300-10C>G
XM_017017671.2:c.712-10C>G	XP_016873160.1:n.712-10C>G
XR_949903.3:n.810-10C>G
NM_002180.3:c.712-10C>G MANE Select	NP_002171.2:n.712-10C>G