Canonical Allele Identifier: CA12239056
Gene: LINC02549 HGNC NCBI

Linked Data

dbSNP Id: rs10455657
gnomAD v2: 6-68984930-T-G
gnomAD v3: 6-68275038-T-G
gnomAD v4: 6-68275038-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.68275038T>G , CM000668.2:g.68275038T>G GRCh38
NC_000006.11:g.68984930T>G , CM000668.1:g.68984930T>G GRCh37
NC_000006.10:g.69041651T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125854.1:n.238-8423A>C