Canonical Allele Identifier: CA1869205552

Gene: LINC01492

Linked Data

• dbSNP Id: rs1827344322
• gnomAD v3: 9-103262123-T-C
• gnomAD v4: 9-103262123-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.103262123T>C , CM000671.2:g.103262123T>C	GRCh38
NC_000009.11:g.106024405T>C , CM000671.1:g.106024405T>C	GRCh37
NC_000009.10:g.105064226T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121578.1:n.771+2401A>G