Canonical Allele Identifier: CA662490622
Gene: MRC1 HGNC NCBI

Linked Data

dbSNP Id: rs1444026645
gnomAD v3: 10-17849941-T-C
gnomAD v4: 10-17849941-T-C
MyVariant Identifiers: chr10:g.17849941T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17849941T>C , CM000672.2:g.17849941T>C GRCh38
NG_047011.1:g.45599T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000569591.3:c.1249+177T>C MANE Select ENSP00000455897.1:n.1249+177T>C
ENST00000569591.2:c.1249+177T>C ENSP00000455897.1:n.1249+177T>C
NM_002438.3:c.1249+177T>C NP_002429.1:n.1249+177T>C
NM_002438.4:c.1249+177T>C MANE Select NP_002429.1:n.1249+177T>C
Search 100 bp 5'
Search 100 bp 3'