Canonical Allele Identifier: CA1127548485

Gene: LINC01492

Linked Data

• dbSNP Id: rs1827341480
• gnomAD v3: 9-103261910-G-T
• gnomAD v4: 9-103261910-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.103261910G>T , CM000671.2:g.103261910G>T	GRCh38
NC_000009.11:g.106024192G>T , CM000671.1:g.106024192G>T	GRCh37
NC_000009.10:g.105064013G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121578.1:n.771+2614C>A