Canonical Allele Identifier: CA15580376
Gene: LINC02906 HGNC NCBI

Linked Data

dbSNP Id: rs278567
gnomAD v2: 8-94169350-T-C
gnomAD v3: 8-93157121-T-C
gnomAD v4: 8-93157121-T-C
MyVariant Identifiers: chr8:g.94169350T>C (hg19) chr8:g.93157121T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.93157121T>C , CM000670.2:g.93157121T>C GRCh38
NC_000008.10:g.94169350T>C , CM000670.1:g.94169350T>C GRCh37
NC_000008.9:g.94238526T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001242668.1:c.37+9610A>G NP_001229597.1:n.37+9610A>G
XR_928416.1:n.60+81T>C
XR_928417.1:n.60+81T>C
XR_928418.1:n.60+81T>C
XR_928419.1:n.60+81T>C
NR_161372.1:n.120+9610A>G
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