Canonical Allele Identifier: CA9376151
Community Standard Title: NM_002361.4(MAG):c.971-5C>T
Gene: MAG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35302443C>T , CM000681.2:g.35302443C>T GRCh38
NC_000019.9:g.35793346C>T , CM000681.1:g.35793346C>T GRCh37
NC_000019.8:g.40485186C>T NCBI36
NG_034078.1:g.15358C>T

Transcript Alleles

HGVS Amino-acid Change
NM_002361.4:c.971-5C>T MANE Select NP_002352.1:n.971-5C>T
ENST00000392213.8:c.971-5C>T MANE Select ENSP00000376048.2:n.971-5C>T
NM_001199216.1:c.896-5C>T NP_001186145.1:n.896-5C>T
NM_001199216.2:c.896-5C>T NP_001186145.1:n.896-5C>T
NM_002361.3:c.971-5C>T NP_002352.1:n.971-5C>T
NM_080600.2:c.971-5C>T NP_542167.1:n.971-5C>T
NM_080600.3:c.971-5C>T NP_542167.1:n.971-5C>T
ENST00000361922.8:c.971-5C>T ENSP00000355234.4:n.971-5C>T
ENST00000392213.7:c.971-5C>T ENSP00000376048.2:n.971-5C>T
ENST00000537831.2:c.896-5C>T ENSP00000440695.1:n.896-5C>T