Canonical Allele Identifier: CA10664127
Gene: LINC01635 HGNC NCBI

Linked Data

dbSNP Id: rs2473307
gnomAD v2: 1-22350834-T-C
gnomAD v3: 1-22024341-T-C
gnomAD v4: 1-22024341-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.22024341T>C , CM000663.2:g.22024341T>C GRCh38
NC_000001.10:g.22350834T>C , CM000663.1:g.22350834T>C GRCh37
NC_000001.9:g.22223421T>C NCBI36
NG_047042.3:g.3831T>C

Transcript Alleles

HGVS Amino-acid change
NR_110692.1:n.351A>G