Canonical Allele Identifier: CA707783959
Gene: MAX HGNC NCBI

Linked Data

dbSNP Id: rs1246337089
gnomAD v3: 14-65075035-C-T
gnomAD v4: 14-65075035-C-T
MyVariant Identifiers: chr14:g.65541753C>T (hg19) chr14:g.65075035C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65075035C>T , CM000676.2:g.65075035C>T GRCh38
NC_000014.8:g.65541753C>T , CM000676.1:g.65541753C>T GRCh37
NC_000014.7:g.64611506C>T NCBI36
NG_029830.1:g.32475G>A , LRG_530:g.32475G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000651648.1:c.145-4666G>A ENSP00000498863.1:n.145-4666G>A
ENST00000341653.6:c.171+18673G>A ENSP00000342482.2:n.171+18673G>A
NM_001271069.1:c.144+18673G>A NP_001257998.1:n.144+18673G>A
NM_197957.3:c.171+18673G>A NP_932061.1:n.171+18673G>A
NM_001271069.2:c.144+18673G>A NP_001257998.1:n.144+18673G>A
NM_197957.4:c.171+18673G>A NP_932061.1:n.171+18673G>A
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