Canonical Allele Identifier: CA15371969
Gene: ADGRV1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10074525

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90914007C>T , CM000667.2:g.90914007C>T GRCh38
NC_000005.9:g.90209824C>T , CM000667.1:g.90209824C>T GRCh37
NC_000005.8:g.90245580C>T NCBI36
NG_007083.1:g.360208C>T
NG_007083.2:g.389664C>T

Transcript Alleles

HGVS Amino-acid change
NM_032119.3:c.17856+50150C>T VV NP_115495.3:p.=
NR_003149.1:n.17869+50150C>T
XM_011543675.1:c.17853+50150C>T XP_011541977.1:p.=
XM_011543676.1:c.17775+50150C>T XP_011541978.1:p.=
XM_011543677.1:c.15159+50150C>T XP_011541979.1:p.=
NM_032119.4:c.17856+50150C>T VV
XM_017009963.2:c.17877+50150C>T XP_016865452.1:p.=
XM_017009964.2:c.17874+50150C>T XP_016865453.1:p.=
XM_017009965.1:c.17874+50150C>T XP_016865454.1:p.=
XM_017009966.2:c.17796+50150C>T XP_016865455.1:p.=
XM_017009967.1:c.17781+50150C>T XP_016865456.1:p.=
XM_017009968.2:c.17697+50150C>T XP_016865457.1:p.=
XM_017009969.2:c.17877+50150C>T XP_016865458.1:p.=
XM_017009972.1:c.10995+50150C>T XP_016865461.1:p.=
XM_017009973.1:c.10974+50150C>T XP_016865462.1:p.=
ENST00000405460.6:c.17856+50150C>T ENSP00000384582.2:p.=
ENST00000425867.2:c.4839+50150C>T ENSP00000392618.2:p.=