Canonical Allele Identifier: CA198811530
Gene: LINC02977 HGNC NCBI
COSMIC:
COSN14794659
COSN17600403
dbSNP:
10125054
gnomAD v2:
9:114798037 G / A
gnomAD v3:
9:112035757 G / A
gnomAD v4:
chr9-112035757-G-A
Joint Max Group AF 0.38213809 (EAS)
Genomes Max Group AF 0.38213809 (EAS)
MyVariant.info:
GRCh38 chr9:g.112035757G>A
GRCh37 chr9:g.114798037G>A
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.112035757G>A , CM000671.2:g.112035757G>A GRCh38
NC_000009.11:g.114798037G>A , CM000671.1:g.114798037G>A GRCh37
NC_000009.10:g.113837858G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930251.3:n.2186+2422C>T
Search 100 bp 5'
Search 100 bp 3'