Canonical Allele Identifier: CA2709645890
Gene: ADGRV1 HGNC NCBI

Linked Data

dbSNP Id: rs2149375697

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90627183T>C , CM000667.2:g.90627183T>C GRCh38
NC_000005.9:g.89923000T>C , CM000667.1:g.89923000T>C GRCh37
NC_000005.8:g.89958756T>C NCBI36
NG_007083.1:g.73384T>C
NG_007083.2:g.102840T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.673-28T>C MANE Select ENSP00000384582.2:n.673-28T>C
ENST00000640083.1:n.378-28T>C
ENST00000640109.1:n.769-28T>C
ENST00000640281.1:n.732-28T>C
ENST00000405460.6:c.673-28T>C ENSP00000384582.2:n.673-28T>C
NM_032119.3:c.673-28T>C NP_115495.3:n.673-28T>C
NR_003149.1:n.769-28T>C
XM_011543675.1:c.673-28T>C XP_011541977.1:n.673-28T>C
XM_011543676.1:c.673-28T>C XP_011541978.1:n.673-28T>C
XM_011543678.1:c.673-28T>C XP_011541980.1:n.673-28T>C
XM_011543679.1:c.673-28T>C XP_011541981.1:n.673-28T>C
NM_032119.4:c.673-28T>C MANE Select NP_115495.3:n.673-28T>C
XM_017009963.2:c.673-28T>C XP_016865452.1:n.673-28T>C
XM_017009964.2:c.673-28T>C XP_016865453.1:n.673-28T>C
XM_017009965.1:c.670-28T>C XP_016865454.1:n.670-28T>C
XM_017009966.2:c.673-28T>C XP_016865455.1:n.673-28T>C
XM_017009967.1:c.577-28T>C XP_016865456.1:n.577-28T>C
XM_017009968.2:c.673-28T>C XP_016865457.1:n.673-28T>C
XM_017009969.2:c.673-28T>C XP_016865458.1:n.673-28T>C
XM_017009970.2:c.673-28T>C XP_016865459.1:n.673-28T>C
XM_017009971.2:c.673-28T>C XP_016865460.1:n.673-28T>C
XM_017009974.2:c.673-28T>C XP_016865463.1:n.673-28T>C
NR_003149.2:n.772-28T>C