Canonical Allele Identifier: CA376196015
Gene: MRC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.17849631C>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17849631C>G , CM000672.2:g.17849631C>G GRCh38
NG_047011.1:g.45289C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000569591.3:c.1116C>G MANE Select ENSP00000455897.1:p.His372Gln
ENST00000569591.2:c.1116C>G ENSP00000455897.1:p.His372Gln
NM_002438.3:c.1116C>G NP_002429.1:p.His372Gln
NM_002438.4:c.1116C>G MANE Select NP_002429.1:p.His372Gln