Canonical Allele Identifier: CA2625288727

Gene: MAX

Linked Data

• gnomAD v4: 14-65075031-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65075031C>A , CM000676.2:g.65075031C>A	GRCh38
NC_000014.8:g.65541749C>A , CM000676.1:g.65541749C>A	GRCh37
NC_000014.7:g.64611502C>A	NCBI36
NG_029830.1:g.32479G>T , LRG_530:g.32479G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000651648.1:c.145-4662G>T	ENSP00000498863.1:n.145-4662G>T
ENST00000341653.6:c.171+18677G>T	ENSP00000342482.2:n.171+18677G>T
NM_001271069.1:c.144+18677G>T	NP_001257998.1:n.144+18677G>T
NM_197957.3:c.171+18677G>T	NP_932061.1:n.171+18677G>T
NM_001271069.2:c.144+18677G>T	NP_001257998.1:n.144+18677G>T
NM_197957.4:c.171+18677G>T	NP_932061.1:n.171+18677G>T