Canonical Allele Identifier: CA106766134
Gene: MAML3 HGNC NCBI

Linked Data

dbSNP Id: rs759090454
MyVariant Identifiers: chr4:g.140795069A>C (hg19) chr4:g.139873915A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.139873915A>C , CM000666.2:g.139873915A>C GRCh38
NC_000004.11:g.140795069A>C , CM000666.1:g.140795069A>C GRCh37
NC_000004.10:g.141014519A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000502696.1:c.111-143248T>G
ENST00000509479.6:c.2079+15442T>G MANE Select ENSP00000421180.1:n.2079+15442T>G
NM_018717.4:c.2067+15442T>G NP_061187.2:n.2067+15442T>G
NM_018717.5:c.2079+15442T>G MANE Select NP_061187.3:n.2079+15442T>G
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