Canonical Allele Identifier: CA591898848
Gene: MRC1 HGNC NCBI

Linked Data

dbSNP Id: rs1397975017
gnomAD v3: 10-17849952-A-G
gnomAD v4: 10-17849952-A-G
MyVariant Identifiers: chr10:g.17849952A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17849952A>G , CM000672.2:g.17849952A>G GRCh38
NG_047011.1:g.45610A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000569591.3:c.1249+188A>G MANE Select ENSP00000455897.1:n.1249+188A>G
ENST00000569591.2:c.1249+188A>G ENSP00000455897.1:n.1249+188A>G
NM_002438.3:c.1249+188A>G NP_002429.1:n.1249+188A>G
NM_002438.4:c.1249+188A>G MANE Select NP_002429.1:n.1249+188A>G
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