Canonical Allele Identifier: CA12444842
Gene: LINC01626 HGNC NCBI

Linked Data

dbSNP Id: rs1727638
gnomAD v2: 6-72139572-G-A
gnomAD v3: 6-71429869-G-A
gnomAD v4: 6-71429869-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.71429869G>A , CM000668.2:g.71429869G>A GRCh38
NC_000006.11:g.72139572G>A , CM000668.1:g.72139572G>A GRCh37
NC_000006.10:g.72196293G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121615.1:n.76-70G>A