Canonical Allele Identifier: CA119707683

Gene: LINC03122

Linked Data

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

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