Canonical Allele Identifier: CA376196374
Gene: MRC1 HGNC NCBI

Linked Data

dbSNP Id: rs1838884376
MyVariant Identifiers: chr10:g.17849697A>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17849697A>T , CM000672.2:g.17849697A>T GRCh38
NG_047011.1:g.45355A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000569591.3:c.1182A>T MANE Select ENSP00000455897.1:p.Glu394Asp
ENST00000569591.2:c.1182A>T ENSP00000455897.1:p.Glu394Asp
NM_002438.3:c.1182A>T NP_002429.1:p.Glu394Asp
NM_002438.4:c.1182A>T MANE Select NP_002429.1:p.Glu394Asp