Canonical Allele Identifier: CA5644677
Gene: DNMBP HGNC NCBI

Linked Data

dbSNP Id: rs3740058
ExAC: 10:101655982 G / A
gnomAD v2: 10-101655982-G-A
gnomAD v3: 10-99896225-G-A
gnomAD v4: 10-99896225-G-A
MyVariant Identifiers: chr10:g.101655982G>A (hg19) chr10:g.99896225G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99896225G>A , CM000672.2:g.99896225G>A GRCh38
NC_000010.10:g.101655982G>A , CM000672.1:g.101655982G>A GRCh37
NC_000010.9:g.101645972G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000324109.9:c.3051+42C>T MANE Select ENSP00000315659.4:n.3051+42C>T
ENST00000543621.6:c.915+42C>T ENSP00000443657.2:n.915+42C>T
ENST00000636706.1:c.1947+42C>T ENSP00000489875.1:n.1947+42C>T
ENST00000324109.8:c.3051+42C>T ENSP00000315659.4:n.3051+42C>T
ENST00000543621.5:c.789+42C>T ENSP00000443657.1:n.789+42C>T
NM_015221.2:c.3051+42C>T NP_056036.1:n.3051+42C>T
XM_006717735.2:c.3051+42C>T XP_006717798.1:n.3051+42C>T
XM_006717736.2:c.2921-1175C>T XP_006717799.1:n.2921-1175C>T
XM_011539559.1:c.3051+42C>T XP_011537861.1:n.3051+42C>T
XM_011539560.1:c.1947+42C>T XP_011537862.1:n.1947+42C>T
NM_001318326.1:c.1947+42C>T NP_001305255.1:n.1947+42C>T
NM_001318327.1:c.915+42C>T NP_001305256.1:n.915+42C>T
NM_015221.3:c.3051+42C>T NP_056036.1:n.3051+42C>T
XM_006717735.3:c.3051+42C>T XP_006717798.1:n.3051+42C>T
XM_011539559.2:c.3051+42C>T XP_011537861.1:n.3051+42C>T
NM_015221.4:c.3051+42C>T MANE Select NP_056036.1:n.3051+42C>T
NM_001318326.2:c.1947+42C>T NP_001305255.1:n.1947+42C>T
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