Canonical Allele Identifier: CA1127548511
Gene: LINC01492 HGNC NCBI

Linked Data

gnomAD v3: 9-103262025-T-C
gnomAD v4: 9-103262025-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.103262025T>C , CM000671.2:g.103262025T>C GRCh38
NC_000009.11:g.106024307T>C , CM000671.1:g.106024307T>C GRCh37
NC_000009.10:g.105064128T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121578.1:n.771+2499A>G
Search 100 bp 5'
Search 100 bp 3'