Canonical Allele Identifier: CA262716050
Gene: MAX HGNC NCBI

Linked Data

dbSNP Id: rs889345455
gnomAD v3: 14-65074865-A-C
gnomAD v4: 14-65074865-A-C
MyVariant Identifiers: chr14:g.65541583A>C (hg19) chr14:g.65074865A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65074865A>C , CM000676.2:g.65074865A>C GRCh38
NC_000014.8:g.65541583A>C , CM000676.1:g.65541583A>C GRCh37
NC_000014.7:g.64611336A>C NCBI36
NG_029830.1:g.32645T>G , LRG_530:g.32645T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000651648.1:c.145-4496T>G ENSP00000498863.1:n.145-4496T>G
ENST00000341653.6:c.171+18843T>G ENSP00000342482.2:n.171+18843T>G
NM_001271069.1:c.144+18843T>G NP_001257998.1:n.144+18843T>G
NM_197957.3:c.171+18843T>G NP_932061.1:n.171+18843T>G
NM_001271069.2:c.144+18843T>G NP_001257998.1:n.144+18843T>G
NM_197957.4:c.171+18843T>G NP_932061.1:n.171+18843T>G
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