Canonical Allele Identifier: CA2142950918
Gene: MAX HGNC NCBI

Linked Data

dbSNP Id: rs2063024007
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65075005C>A , CM000676.2:g.65075005C>A GRCh38
NC_000014.8:g.65541723C>A , CM000676.1:g.65541723C>A GRCh37
NC_000014.7:g.64611476C>A NCBI36
NG_029830.1:g.32505G>T , LRG_530:g.32505G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000651648.1:c.145-4636G>T ENSP00000498863.1:n.145-4636G>T
ENST00000341653.6:c.171+18703G>T ENSP00000342482.2:n.171+18703G>T
NM_001271069.1:c.144+18703G>T NP_001257998.1:n.144+18703G>T
NM_197957.3:c.171+18703G>T NP_932061.1:n.171+18703G>T
NM_001271069.2:c.144+18703G>T NP_001257998.1:n.144+18703G>T
NM_197957.4:c.171+18703G>T NP_932061.1:n.171+18703G>T
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