Canonical Allele Identifier: CA408940149
Gene: MAFB HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.39316595T>A (hg19) chr20:g.40687955T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.40687955T>A , CM000682.2:g.40687955T>A GRCh38
NC_000020.10:g.39316595T>A , CM000682.1:g.39316595T>A GRCh37
NC_000020.9:g.38750009T>A NCBI36
NG_023378.1:g.6282A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000373313.3:c.896A>T MANE Select ENSP00000362410.2:p.Glu299Val
ENST00000373313.2:c.896A>T ENSP00000362410.2:p.Glu299Val
NM_005461.4:c.896A>T NP_005452.2:p.Glu299Val
NM_005461.5:c.896A>T MANE Select NP_005452.2:p.Glu299Val
Search 100 bp 5'
Search 100 bp 3'