Canonical Allele Identifier: CA381649432

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68700939C>A (hg19) ; chr11:g.68933471C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68933471C>A , CM000673.2:g.68933471C>A	GRCh38
NC_000011.9:g.68700939C>A , CM000673.1:g.68700939C>A	GRCh37
NC_000011.8:g.68457515C>A	NCBI36
NG_007976.1:g.34621C>A , LRG_250:g.34621C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.1408C>A MANE Select	ENSP00000255078.4:p.His470Asn
ENST00000536803.2:n.319C>A
ENST00000674955.1:c.*125C>A	ENSP00000502463.1:n.*125C>A
ENST00000675118.1:c.896C>A
ENST00000675205.1:n.173C>A
ENST00000675310.1:n.545C>A
ENST00000675615.1:c.1408C>A	ENSP00000502413.1:p.His470Asn
ENST00000675648.1:n.783C>A
ENST00000675997.1:n.113-993C>A
ENST00000676149.1:n.482C>A
ENST00000676173.1:n.2153C>A
ENST00000676228.1:c.*731C>A	ENSP00000502375.1:n.*731C>A
ENST00000255078.7:c.1408C>A	ENSP00000255078.3:p.His470Asn
ENST00000537458.5:n.525C>A
ENST00000539064.5:n.1167C>A
ENST00000543739.5:n.525C>A
NM_002180.2:c.1408C>A , LRG_250t1:c.1408C>A	NP_002171.2:p.His470Asn
XM_005273974.2:c.397C>A	XP_005274031.1:p.His133Asn
XM_005273975.2:c.280C>A	XP_005274032.1:p.His94Asn
XM_011544994.1:c.175C>A	XP_011543296.1:p.His59Asn
XR_949903.1:n.1510C>A
XM_005273975.3:c.280C>A	XP_005274032.1:p.His94Asn
XM_017017669.2:c.397C>A	XP_016873158.1:p.His133Asn
XM_017017670.2:c.397C>A	XP_016873159.1:p.His133Asn
XM_017017671.2:c.1408C>A	XP_016873160.1:p.His470Asn
XR_949903.3:n.1506C>A
NM_002180.3:c.1408C>A MANE Select	NP_002171.2:p.His470Asn