Canonical Allele Identifier: CA12228331
Gene: LINC02828 HGNC NCBI

Linked Data

dbSNP Id: rs17419851
gnomAD v2: 6-24749413-C-T
gnomAD v3: 6-24749185-C-T
gnomAD v4: 6-24749185-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24749185C>T , CM000668.2:g.24749185C>T GRCh38
NC_000006.11:g.24749413C>T , CM000668.1:g.24749413C>T GRCh37
NC_000006.10:g.24857392C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926603.1:n.198+37C>T
XR_926603.2:n.198+37C>T