Canonical Allele Identifier: CA308568967

Gene: RPS19 MIR6797

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41869697A>G , CM000681.2:g.41869697A>G	GRCh38
NC_000019.9:g.42373767A>G , CM000681.1:g.42373767A>G	GRCh37
NC_000019.8:g.47065607A>G	NCBI36
NG_007080.2:g.14780A>G
NG_007080.3:g.14780A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001022.4:c.357-2A>G (RPS19) MANE Select	NP_001013.1:n.357-2A>G
ENST00000598742.6:c.357-2A>G (RPS19) MANE Select	ENSP00000470972.1:n.357-2A>G
NM_001022.3:c.357-2A>G (RPS19)	NP_001013.1:n.357-2A>G
NM_001321483.1:c.357-2A>G (RPS19)	NP_001308412.1:n.357-2A>G
NM_001321483.2:c.357-2A>G (RPS19)	NP_001308412.1:n.357-2A>G
NM_001321484.1:c.357-2A>G (RPS19)	NP_001308413.1:n.357-2A>G
NM_001321484.2:c.357-2A>G (RPS19)	NP_001308413.1:n.357-2A>G
NM_001321485.1:c.370-2A>G (RPS19)	NP_001308414.1:n.370-2A>G
NM_001321485.2:c.370-2A>G (RPS19)	NP_001308414.1:n.370-2A>G
NR_106855.1:n.71A>G (MIR6797)
ENST00000221975.6:c.135-2A>G (RPS19)	ENSP00000221975.2:n.135-2A>G
ENST00000593863.5:c.357-2A>G (RPS19)	ENSP00000470004.1:n.357-2A>G
ENST00000598742.5:c.357-2A>G (RPS19)	ENSP00000470972.1:n.357-2A>G
ENST00000600467.6:c.357-2A>G (RPS19)	ENSP00000469228.2:n.357-2A>G
XM_017027113.2:c.357-2A>G (RPS19)	XP_016882602.1:n.357-2A>G