Canonical Allele Identifier: CA707783996
Gene: MAX HGNC NCBI

Linked Data

dbSNP Id: rs1490183400

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65075109G>A , CM000676.2:g.65075109G>A GRCh38
NC_000014.8:g.65541827G>A , CM000676.1:g.65541827G>A GRCh37
NC_000014.7:g.64611580G>A NCBI36
NG_029830.1:g.32401C>T , LRG_530:g.32401C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000651648.1:c.145-4740C>T ENSP00000498863.1:n.145-4740C>T
ENST00000341653.6:c.171+18599C>T ENSP00000342482.2:n.171+18599C>T
NM_001271069.1:c.144+18599C>T NP_001257998.1:n.144+18599C>T
NM_197957.3:c.171+18599C>T NP_932061.1:n.171+18599C>T
NM_001271069.2:c.144+18599C>T NP_001257998.1:n.144+18599C>T
NM_197957.4:c.171+18599C>T NP_932061.1:n.171+18599C>T