Canonical Allele Identifier: CA589962220

Gene: LINC01492

Linked Data

• dbSNP Id: rs1273260483
• gnomAD v2: 9-106024363-G-C
• gnomAD v3: 9-103262081-G-C
• gnomAD v4: 9-103262081-G-C
• MyVariant Identifiers: chr9:g.106024363G>C (hg19) ; chr9:g.103262081G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.103262081G>C , CM000671.2:g.103262081G>C	GRCh38
NC_000009.11:g.106024363G>C , CM000671.1:g.106024363G>C	GRCh37
NC_000009.10:g.105064184G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121578.1:n.771+2443C>G