Canonical Allele Identifier: CA468508624
Gene: MRC1 HGNC NCBI

Linked Data

dbSNP Id: rs1476655479
MyVariant Identifiers: chr10:g.17849757A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17849757A>G , CM000672.2:g.17849757A>G GRCh38
NG_047011.1:g.45415A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000569591.3:c.1242A>G MANE Select ENSP00000455897.1:p.Leu414=
ENST00000569591.2:c.1242A>G ENSP00000455897.1:p.Leu414=
NM_002438.3:c.1242A>G NP_002429.1:p.Leu414=
NM_002438.4:c.1242A>G MANE Select NP_002429.1:p.Leu414=