Canonical Allele Identifier: CA2142950856
Gene: MAX HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65074822A= , CM000676.2:g.65074822A= GRCh38
NC_000014.8:g.65541540A= , CM000676.1:g.65541540A= GRCh37
NC_000014.7:g.64611293A= NCBI36
NG_029830.1:g.32688T= , LRG_530:g.32688T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000651648.1:c.145-4453T= ENSP00000498863.1:n.145-4453T=
ENST00000341653.6:c.171+18886T= ENSP00000342482.2:n.171+18886T=
NM_001271069.1:c.144+18886T= NP_001257998.1:n.144+18886T=
NM_197957.3:c.171+18886T= NP_932061.1:n.171+18886T=
NM_001271069.2:c.144+18886T= NP_001257998.1:n.144+18886T=
NM_197957.4:c.171+18886T= NP_932061.1:n.171+18886T=
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