Canonical Allele Identifier: CA15417891

Gene: LINC03122

Linked Data

• dbSNP Id: rs11738335
• gnomAD v2: 5-60950211-T-G
• gnomAD v3: 5-61654384-T-G
• gnomAD v4: 5-61654384-T-G
• MyVariant Identifiers: chr5:g.60950211T>G (hg19) ; chr5:g.61654384T>G (hg38)

Genomic Alleles

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

Transcript Alleles

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