Canonical Allele Identifier: CA662490649
Gene: MRC1 HGNC NCBI

Linked Data

dbSNP Id: rs1445605274
MyVariant Identifiers: chr10:g.17849995A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17849995A>T , CM000672.2:g.17849995A>T GRCh38
NG_047011.1:g.45653A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000569591.3:c.1249+231A>T MANE Select ENSP00000455897.1:n.1249+231A>T
ENST00000569591.2:c.1249+231A>T ENSP00000455897.1:n.1249+231A>T
NM_002438.3:c.1249+231A>T NP_002429.1:n.1249+231A>T
NM_002438.4:c.1249+231A>T MANE Select NP_002429.1:n.1249+231A>T
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