Canonical Allele Identifier: CA381652632
Gene: IGHMBP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68936495C>G , CM000673.2:g.68936495C>G GRCh38
NC_000011.9:g.68703963C>G , CM000673.1:g.68703963C>G GRCh37
NC_000011.8:g.68460539C>G NCBI36
NG_007976.1:g.37645C>G , LRG_250:g.37645C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000255078.8:c.2015C>G MANE Select ENSP00000255078.4:p.Ser672Cys
ENST00000674675.1:c.259C>G
ENST00000674878.1:c.259C>G
ENST00000674955.1:c.*732C>G ENSP00000502463.1:n.*732C>G
ENST00000675118.1:c.1503C>G
ENST00000675389.1:n.290C>G
ENST00000675615.1:c.2015C>G ENSP00000502413.1:p.Ser672Cys
ENST00000675648.1:n.1390C>G
ENST00000675916.1:c.259C>G
ENST00000676173.1:n.2760C>G
ENST00000676182.1:c.446C>G
ENST00000676228.1:c.*1338C>G ENSP00000502375.1:n.*1338C>G
ENST00000255078.7:c.2015C>G ENSP00000255078.3:p.Ser672Cys
ENST00000539064.5:n.1774C>G
ENST00000543739.5:n.1008C>G
NM_002180.2:c.2015C>G , LRG_250t1:c.2015C>G NP_002171.2:p.Ser672Cys
XM_005273974.2:c.1004C>G XP_005274031.1:p.Ser335Cys
XM_005273975.2:c.887C>G XP_005274032.1:p.Ser296Cys
XM_011544994.1:c.782C>G XP_011543296.1:p.Ser261Cys
XR_949903.1:n.2117C>G
XM_005273975.3:c.887C>G XP_005274032.1:p.Ser296Cys
XM_017017669.2:c.1004C>G XP_016873158.1:p.Ser335Cys
XM_017017670.2:c.1004C>G XP_016873159.1:p.Ser335Cys
XR_949903.3:n.2113C>G
NM_002180.3:c.2015C>G MANE Select NP_002171.2:p.Ser672Cys