Canonical Allele Identifier: CA14627134
Gene: LINC00907 HGNC NCBI
dbSNP:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.42525692T>C , CM000680.2:g.42525692T>C GRCh38
NC_000018.9:g.40105657T>C , CM000680.1:g.40105657T>C GRCh37
NC_000018.8:g.38359655T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046174.2:n.873-49101T>C
NR_046454.1:n.704-7427T>C