Canonical Allele Identifier: CA2614748051
Gene: IGHMBP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68936201G>C , CM000673.2:g.68936201G>C GRCh38
NC_000011.9:g.68703669G>C , CM000673.1:g.68703669G>C GRCh37
NC_000011.8:g.68460245G>C NCBI36
NG_007976.1:g.37351G>C , LRG_250:g.37351G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000255078.8:c.1757-36G>C MANE Select ENSP00000255078.4:n.1757-36G>C
ENST00000674955.1:c.*474-36G>C ENSP00000502463.1:n.*474-36G>C
ENST00000675118.1:c.1245-36G>C
ENST00000675389.1:n.32-36G>C
ENST00000675615.1:c.1757-36G>C ENSP00000502413.1:n.1757-36G>C
ENST00000675648.1:n.1132-36G>C
ENST00000676173.1:n.2502-36G>C
ENST00000676182.1:c.188-36G>C
ENST00000676228.1:c.*1080-36G>C ENSP00000502375.1:n.*1080-36G>C
ENST00000255078.7:c.1757-36G>C ENSP00000255078.3:n.1757-36G>C
ENST00000539064.5:n.1516-36G>C
ENST00000541229.5:n.452-36G>C
ENST00000543739.5:n.750-36G>C
ENST00000545475.1:n.353-36G>C
NM_002180.2:c.1757-36G>C , LRG_250t1:c.1757-36G>C NP_002171.2:n.1757-36G>C
XM_005273974.2:c.746-36G>C XP_005274031.1:n.746-36G>C
XM_005273975.2:c.629-36G>C XP_005274032.1:n.629-36G>C
XM_011544994.1:c.524-36G>C XP_011543296.1:n.524-36G>C
XR_949903.1:n.1859-36G>C
XM_005273975.3:c.629-36G>C XP_005274032.1:n.629-36G>C
XM_017017669.2:c.746-36G>C XP_016873158.1:n.746-36G>C
XM_017017670.2:c.746-36G>C XP_016873159.1:n.746-36G>C
XR_949903.3:n.1855-36G>C
NM_002180.3:c.1757-36G>C MANE Select NP_002171.2:n.1757-36G>C