Canonical Allele Identifier: CA964079240
Gene: MAX HGNC NCBI

Linked Data

dbSNP Id: rs1384689794

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65074922C>A , CM000676.2:g.65074922C>A GRCh38
NC_000014.8:g.65541640C>A , CM000676.1:g.65541640C>A GRCh37
NC_000014.7:g.64611393C>A NCBI36
NG_029830.1:g.32588G>T , LRG_530:g.32588G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000651648.1:c.145-4553G>T ENSP00000498863.1:n.145-4553G>T
ENST00000341653.6:c.171+18786G>T ENSP00000342482.2:n.171+18786G>T
NM_001271069.1:c.144+18786G>T NP_001257998.1:n.144+18786G>T
NM_197957.3:c.171+18786G>T NP_932061.1:n.171+18786G>T
NM_001271069.2:c.144+18786G>T NP_001257998.1:n.144+18786G>T
NM_197957.4:c.171+18786G>T NP_932061.1:n.171+18786G>T