Canonical Allele Identifier: CA2142950920
Gene: MAX HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65075008G= , CM000676.2:g.65075008G= GRCh38
NC_000014.8:g.65541726G= , CM000676.1:g.65541726G= GRCh37
NC_000014.7:g.64611479G= NCBI36
NG_029830.1:g.32502C= , LRG_530:g.32502C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000651648.1:c.145-4639C= ENSP00000498863.1:n.145-4639C=
ENST00000341653.6:c.171+18700C= ENSP00000342482.2:n.171+18700C=
NM_001271069.1:c.144+18700C= NP_001257998.1:n.144+18700C=
NM_197957.3:c.171+18700C= NP_932061.1:n.171+18700C=
NM_001271069.2:c.144+18700C= NP_001257998.1:n.144+18700C=
NM_197957.4:c.171+18700C= NP_932061.1:n.171+18700C=
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