Canonical Allele Identifier: CA897872070
Gene: LRRC58 HGNC NCBI

Linked Data

dbSNP Id: rs1262334320
MyVariant Identifiers: chr3:g.120043887C>G (hg19) chr3:g.120325040C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.120325040C>G , CM000665.2:g.120325040C>G GRCh38
NC_000003.11:g.120043887C>G , CM000665.1:g.120043887C>G GRCh37
NC_000003.10:g.121526577C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000295628.4:c.*6160G>C MANE Select ENSP00000295628.3:n.*6160G>C
ENST00000295628.3:c.*6160G>C ENSP00000295628.3:n.*6160G>C
NM_001099678.1:c.*6160G>C NP_001093148.1:n.*6160G>C
NM_001099678.2:c.*6160G>C MANE Select NP_001093148.1:n.*6160G>C
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