Canonical Allele Identifier: CA2142950871
Gene: MAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65074885A= , CM000676.2:g.65074885A= GRCh38
NC_000014.8:g.65541603A= , CM000676.1:g.65541603A= GRCh37
NC_000014.7:g.64611356A= NCBI36
NG_029830.1:g.32625T= , LRG_530:g.32625T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000651648.1:c.145-4516T= ENSP00000498863.1:n.145-4516T=
ENST00000341653.6:c.171+18823T= ENSP00000342482.2:n.171+18823T=
NM_001271069.1:c.144+18823T= NP_001257998.1:n.144+18823T=
NM_197957.3:c.171+18823T= NP_932061.1:n.171+18823T=
NM_001271069.2:c.144+18823T= NP_001257998.1:n.144+18823T=
NM_197957.4:c.171+18823T= NP_932061.1:n.171+18823T=