Canonical Allele Identifier: CA381651724

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68703802C>G (hg19) ; chr11:g.68936334C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936334C>G , CM000673.2:g.68936334C>G	GRCh38
NC_000011.9:g.68703802C>G , CM000673.1:g.68703802C>G	GRCh37
NC_000011.8:g.68460378C>G	NCBI36
NG_007976.1:g.37484C>G , LRG_250:g.37484C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.1854C>G MANE Select	ENSP00000255078.4:p.Asn618Lys
ENST00000674675.1:c.98C>G
ENST00000674878.1:c.98C>G
ENST00000674955.1:c.*571C>G	ENSP00000502463.1:n.*571C>G
ENST00000675118.1:c.1342C>G
ENST00000675389.1:n.129C>G
ENST00000675615.1:c.1854C>G	ENSP00000502413.1:p.Asn618Lys
ENST00000675648.1:n.1229C>G
ENST00000675916.1:c.98C>G
ENST00000676173.1:n.2599C>G
ENST00000676182.1:c.285C>G
ENST00000676228.1:c.*1177C>G	ENSP00000502375.1:n.*1177C>G
ENST00000255078.7:c.1854C>G	ENSP00000255078.3:p.Asn618Lys
ENST00000539064.5:n.1613C>G
ENST00000541229.5:n.549C>G
ENST00000543739.5:n.847C>G
ENST00000545475.1:n.450C>G
NM_002180.2:c.1854C>G , LRG_250t1:c.1854C>G	NP_002171.2:p.Asn618Lys
XM_005273974.2:c.843C>G	XP_005274031.1:p.Asn281Lys
XM_005273975.2:c.726C>G	XP_005274032.1:p.Asn242Lys
XM_011544994.1:c.621C>G	XP_011543296.1:p.Asn207Lys
XR_949903.1:n.1956C>G
XM_005273975.3:c.726C>G	XP_005274032.1:p.Asn242Lys
XM_017017669.2:c.843C>G	XP_016873158.1:p.Asn281Lys
XM_017017670.2:c.843C>G	XP_016873159.1:p.Asn281Lys
XR_949903.3:n.1952C>G
NM_002180.3:c.1854C>G MANE Select	NP_002171.2:p.Asn618Lys