Canonical Allele Identifier: CA2625288731
Gene: MAX HGNC NCBI

Linked Data

gnomAD v4: 14-65075044-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65075044A>G , CM000676.2:g.65075044A>G GRCh38
NC_000014.8:g.65541762A>G , CM000676.1:g.65541762A>G GRCh37
NC_000014.7:g.64611515A>G NCBI36
NG_029830.1:g.32466T>C , LRG_530:g.32466T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000651648.1:c.145-4675T>C ENSP00000498863.1:n.145-4675T>C
ENST00000341653.6:c.171+18664T>C ENSP00000342482.2:n.171+18664T>C
NM_001271069.1:c.144+18664T>C NP_001257998.1:n.144+18664T>C
NM_197957.3:c.171+18664T>C NP_932061.1:n.171+18664T>C
NM_001271069.2:c.144+18664T>C NP_001257998.1:n.144+18664T>C
NM_197957.4:c.171+18664T>C NP_932061.1:n.171+18664T>C
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