Canonical Allele Identifier: CA376196641
Gene: MRC1 HGNC NCBI

Linked Data

dbSNP Id: rs1838885593
gnomAD v4: 10-17849746-A-G
MyVariant Identifiers: chr10:g.17849746A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17849746A>G , CM000672.2:g.17849746A>G GRCh38
NG_047011.1:g.45404A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000569591.3:c.1231A>G MANE Select ENSP00000455897.1:p.Ile411Val
ENST00000569591.2:c.1231A>G ENSP00000455897.1:p.Ile411Val
NM_002438.3:c.1231A>G NP_002429.1:p.Ile411Val
NM_002438.4:c.1231A>G MANE Select NP_002429.1:p.Ile411Val
Search 100 bp 5'
Search 100 bp 3'