Canonical Allele Identifier: CA1550332474
Gene: LINC03122 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.61654424T= , CM000667.2:g.61654424T= GRCh38
NC_000005.9:g.60950251T= , CM000667.1:g.60950251T= GRCh37
NC_000005.8:g.60986008T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_173667.3:c.37+11024T= NP_775938.1:n.37+11024T=
NR_126523.1:n.140+11024T=
NR_126524.1:n.140+11024T=
NR_126525.1:n.66+16578T=
XM_017009382.1:c.1+17056T= XP_016864871.1:n.1+17056T=
NR_161251.1:n.161+11024T=