Canonical Allele Identifier: CA376196191
Gene: MRC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.17849662A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17849662A>C , CM000672.2:g.17849662A>C GRCh38
NG_047011.1:g.45320A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000569591.3:c.1147A>C MANE Select ENSP00000455897.1:p.Ile383Leu
ENST00000569591.2:c.1147A>C ENSP00000455897.1:p.Ile383Leu
NM_002438.3:c.1147A>C NP_002429.1:p.Ile383Leu
NM_002438.4:c.1147A>C MANE Select NP_002429.1:p.Ile383Leu
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Search 100 bp 3'