Canonical Allele Identifier: CA2625288722
Gene: MAX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65075024T>C , CM000676.2:g.65075024T>C GRCh38
NC_000014.8:g.65541742T>C , CM000676.1:g.65541742T>C GRCh37
NC_000014.7:g.64611495T>C NCBI36
NG_029830.1:g.32486A>G , LRG_530:g.32486A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000651648.1:c.145-4655A>G ENSP00000498863.1:n.145-4655A>G
ENST00000341653.6:c.171+18684A>G ENSP00000342482.2:n.171+18684A>G
NM_001271069.1:c.144+18684A>G NP_001257998.1:n.144+18684A>G
NM_197957.3:c.171+18684A>G NP_932061.1:n.171+18684A>G
NM_001271069.2:c.144+18684A>G NP_001257998.1:n.144+18684A>G
NM_197957.4:c.171+18684A>G NP_932061.1:n.171+18684A>G