Canonical Allele Identifier: CA955792913

Linked Data

dbSNP Id: rs1949039773

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48423630G>A , CM000675.2:g.48423630G>A GRCh38
NC_000013.10:g.48997766G>A , CM000675.1:g.48997766G>A GRCh37
NC_000013.9:g.47895767G>A NCBI36
NG_009009.1:g.124884G>A , LRG_517:g.124884G>A
NG_012874.1:g.26075C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000267163.6:c.1696-29363G>A (RB1) MANE Select ENSP00000267163.4:n.1696-29363G>A
ENST00000643064.1:c.194+42187G>A (RB1)
ENST00000650461.1:c.1696-29363G>A (RB1) ENSP00000497193.1:n.1696-29363G>A
ENST00000267163.4:c.1696-29363G>A (RB1) ENSP00000267163.4:n.1696-29363G>A
ENST00000345941.2:c.-1094-840C>T (LPAR6) ENSP00000344353.2:n.-1094-840C>T
ENST00000378434.8:c.-1347+363C>T (LPAR6) ENSP00000367691.3:n.-1347+363C>T
ENST00000465365.6:n.662+363C>T (LPAR6)
NM_000321.2:c.1696-29363G>A , LRG_517t1:c.1696-29363G>A (RB1) NP_000312.2:n.1696-29363G>A
NM_001162497.1:c.-1094-840C>T (LPAR6) NP_001155969.1:n.-1094-840C>T
NM_005767.5:c.-1347+363C>T (LPAR6) NP_005758.2:n.-1347+363C>T
XM_011535171.1:c.1435-29363G>A (RB1) XP_011533473.1:n.1435-29363G>A
XM_011535171.2:c.1435-29363G>A (RB1) XP_011533473.1:n.1435-29363G>A
NM_001162497.2:c.-1094-840C>T (LPAR6) NP_001155969.1:n.-1094-840C>T
NM_001377316.1:c.-1094-840C>T (LPAR6) NP_001364245.1:n.-1094-840C>T
NM_001377317.1:c.-1094-840C>T (LPAR6) NP_001364246.1:n.-1094-840C>T
NM_005767.6:c.-1347+363C>T (LPAR6) NP_005758.2:n.-1347+363C>T
NM_000321.3:c.1696-29363G>A (RB1) MANE Select NP_000312.2:n.1696-29363G>A
NM_001162497.3:c.-1094-840C>T (LPAR6) NP_001155969.1:n.-1094-840C>T
NM_001377316.2:c.-1094-840C>T (LPAR6) NP_001364245.1:n.-1094-840C>T
NM_001377317.2:c.-1094-840C>T (LPAR6) NP_001364246.1:n.-1094-840C>T
NM_005767.7:c.-1347+363C>T (LPAR6) NP_005758.2:n.-1347+363C>T