Canonical Allele Identifier: CA14701936
Gene: MAG HGNC NCBI

Linked Data

dbSNP Id: rs720308

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35307157A>G , CM000681.2:g.35307157A>G GRCh38
NC_000019.9:g.35798060A>G , CM000681.1:g.35798060A>G GRCh37
NC_000019.8:g.40489900A>G NCBI36
NG_034078.1:g.20072A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000392213.8:c.1232-2717A>G MANE Select ENSP00000376048.2:n.1232-2717A>G
ENST00000361922.8:c.1232-2717A>G ENSP00000355234.4:n.1232-2717A>G
ENST00000392213.7:c.1232-2717A>G ENSP00000376048.2:n.1232-2717A>G
ENST00000537831.2:c.1157-2717A>G ENSP00000440695.1:n.1157-2717A>G
NM_001199216.1:c.1157-2717A>G NP_001186145.1:n.1157-2717A>G
NM_002361.3:c.1232-2717A>G NP_002352.1:n.1232-2717A>G
NM_080600.2:c.1232-2717A>G NP_542167.1:n.1232-2717A>G
NM_002361.4:c.1232-2717A>G MANE Select NP_002352.1:n.1232-2717A>G
NM_001199216.2:c.1157-2717A>G NP_001186145.1:n.1157-2717A>G
NM_080600.3:c.1232-2717A>G NP_542167.1:n.1232-2717A>G