Canonical Allele Identifier: CA1040222528

Gene: LINC01473

Linked Data

• dbSNP Id: rs2046593
• gnomAD v3: 2-186079936-C-G
• gnomAD v4: 2-186079936-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.186079936C>G , CM000664.2:g.186079936C>G	GRCh38
NC_000002.11:g.186944663C>G , CM000664.1:g.186944663C>G	GRCh37
NC_000002.10:g.186652908C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_110218.1:n.172+1394G>C