Canonical Allele Identifier: CA249285800

Identifiers and link-outs to other resources

dbSNP Id: rs2227311

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48412896A>G , CM000675.2:g.48412896A>G GRCh38
NC_000013.9:g.47885033A>G NCBI36
NC_000013.10:g.48987032A>G , CM000675.1:g.48987032A>G GRCh37
NG_009009.1:g.114150A>G , LRG_517:g.114150A>G
NG_012874.1:g.36809T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000267163.4:c.1695+31453A>G ENSP00000267163.4:p.=
ENST00000345941.2:c.-473T>C ENSP00000344353.2:p.=
ENST00000378434.8:c.-473T>C ENSP00000367691.3:p.=
ENST00000462781.5:n.114+2804T>C
ENST00000465365.6:n.1068+2804T>C
ENST00000470937.1:n.117+2804T>C
ENST00000620633.4:c.-473T>C ENSP00000482660.1:p.=
NM_000321.2:c.1695+31453A>G , LRG_517t1:c.1695+31453A>G (RB1) NP_000312.2:p.=
NM_001162497.1:c.-473T>C (LPAR6) VV NP_001155969.1:p.=
NM_001162498.1:c.-473T>C (LPAR6) VV NP_001155970.1:p.=
NM_005767.5:c.-473T>C (LPAR6) VV NP_005758.2:p.=
XM_011535171.1:c.1434+31453A>G (RB1) XP_011533473.1:p.=
XM_011535171.2:c.1434+31453A>G (RB1)
XM_024449302.1:c.-473T>C (LPAR6) XP_024305070.1:p.=
XM_024449303.1:c.192+2804T>C (LPAR6) XP_024305071.1:p.=
XM_024449304.1:c.192+2804T>C (LPAR6) XP_024305072.1:p.=