Canonical Allele Identifier: CA262716109

Gene: MAX

Linked Data

• dbSNP Id: rs1023526097
• gnomAD v3: 14-65075048-T-C
• gnomAD v4: 14-65075048-T-C
• MyVariant Identifiers: chr14:g.65541766T>C (hg19) ; chr14:g.65075048T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65075048T>C , CM000676.2:g.65075048T>C	GRCh38
NC_000014.8:g.65541766T>C , CM000676.1:g.65541766T>C	GRCh37
NC_000014.7:g.64611519T>C	NCBI36
NG_029830.1:g.32462A>G , LRG_530:g.32462A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000651648.1:c.145-4679A>G	ENSP00000498863.1:n.145-4679A>G
ENST00000341653.6:c.171+18660A>G	ENSP00000342482.2:n.171+18660A>G
NM_001271069.1:c.144+18660A>G	NP_001257998.1:n.144+18660A>G
NM_197957.3:c.171+18660A>G	NP_932061.1:n.171+18660A>G
NM_001271069.2:c.144+18660A>G	NP_001257998.1:n.144+18660A>G
NM_197957.4:c.171+18660A>G	NP_932061.1:n.171+18660A>G