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_000005.8:g.90245580C>T NCBI36
NC_000005.9:g.90209824C>T , CM000667.1:g.90209824C>T GRCh37
NG_007083.1:g.360208C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000405460.6:c.17856+50150C>T ENSP00000384582.2:p.=
ENST00000425867.2:c.4839+50150C>T ENSP00000392618.2:p.=
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.=