Canonical Allele Identifier: CA468508621
Gene: MRC1 HGNC NCBI

Linked Data

dbSNP Id: rs1838885738

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17849754G>A , CM000672.2:g.17849754G>A GRCh38
NG_047011.1:g.45412G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000569591.3:c.1239G>A MANE Select ENSP00000455897.1:p.Gln413=
ENST00000569591.2:c.1239G>A ENSP00000455897.1:p.Gln413=
NM_002438.3:c.1239G>A NP_002429.1:p.Gln413=
NM_002438.4:c.1239G>A MANE Select NP_002429.1:p.Gln413=