Canonical Allele Identifier: CA376196604
Gene: MRC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.17849738A>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17849738A>C , CM000672.2:g.17849738A>C GRCh38
NG_047011.1:g.45396A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000569591.3:c.1223A>C MANE Select ENSP00000455897.1:p.Asp408Ala
ENST00000569591.2:c.1223A>C ENSP00000455897.1:p.Asp408Ala
NM_002438.3:c.1223A>C NP_002429.1:p.Asp408Ala
NM_002438.4:c.1223A>C MANE Select NP_002429.1:p.Asp408Ala