Canonical Allele Identifier: CA1127548490

Gene: LINC01492

Linked Data

• dbSNP Id: rs1827342234
• gnomAD v3: 9-103261933-T-G
• gnomAD v4: 9-103261933-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.103261933T>G , CM000671.2:g.103261933T>G	GRCh38
NC_000009.11:g.106024215T>G , CM000671.1:g.106024215T>G	GRCh37
NC_000009.10:g.105064036T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121578.1:n.771+2591A>C