Canonical Allele Identifier: CA119707683
Gene: LINC03122 HGNC NCBI
MyVariant.info:
GRCh38 chr5:g.61654384T>C
GRCh37 chr5:g.60950211T>C
gnomAD v3:
5:61654384 T / C
gnomAD v4:
chr5-61654384-T-C
Joint Max Group AF 0.00003257 (AFR)
Genomes Max Group AF 0.00003257 (AFR)
dbSNP:
11738335
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.61654384T>C , CM000667.2:g.61654384T>C GRCh38
NC_000005.9:g.60950211T>C , CM000667.1:g.60950211T>C GRCh37
NC_000005.8:g.60985968T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_173667.3:c.37+10984T>C NP_775938.1:n.37+10984T>C
NR_126523.1:n.140+10984T>C
NR_126524.1:n.140+10984T>C
NR_126525.1:n.66+16538T>C
XM_017009382.1:c.1+17016T>C XP_016864871.1:n.1+17016T>C
NR_161251.1:n.161+10984T>C
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