Canonical Allele Identifier: CA2466520895

Linked Data

dbSNP Id: rs2064971193

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153906735G>T , CM000685.2:g.153906735G>T GRCh38
NC_000023.10:g.153172189G>T , CM000685.1:g.153172189G>T GRCh37
NC_000023.9:g.152825383G>T NCBI36
NG_008687.1:g.6762G>T
NG_009645.3:g.7489C>A
NG_013220.1:g.24526C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000646375.2:c.*7G>T (AVPR2) MANE Select ENSP00000496396.1:n.*7G>T
ENST00000434679.6:c.*489G>T (AVPR2) ENSP00000393397.1:n.*489G>T
ENST00000642393.1:c.97+2335C>A
ENST00000646191.1:c.97+2335C>A
ENST00000646375.1:c.*7G>T (AVPR2) ENSP00000496396.1:n.*7G>T
ENST00000337474.5:c.*7G>T (AVPR2) ENSP00000338072.5:n.*7G>T
ENST00000358927.6:c.*7G>T (AVPR2) ENSP00000351805.2:n.*7G>T
ENST00000370049.1:c.*299G>T (AVPR2) ENSP00000359066.1:n.*299G>T
ENST00000430697.1:c.1035G>T (AVPR2) ENSP00000393513.1:p.Leu345=
ENST00000434679.5:c.*489G>T (AVPR2) ENSP00000393397.1:n.*489G>T
ENST00000464967.5:n.154+2335C>A (L1CAM)
NM_000054.4:c.*7G>T (AVPR2) NP_000045.1:n.*7G>T
NM_001146151.1:c.*299G>T (AVPR2) NP_001139623.1:n.*299G>T
NR_027419.1:n.1170G>T (AVPR2)
XM_006724828.2:c.*7G>T (AVPR2) XP_006724891.1:n.*7G>T
NM_000054.5:c.*7G>T (AVPR2) NP_000045.1:n.*7G>T
NM_001146151.2:c.*299G>T (AVPR2) NP_001139623.1:n.*299G>T
XM_006724828.3:c.*7G>T (AVPR2) XP_006724891.1:n.*7G>T
NM_000054.6:c.*7G>T (AVPR2) NP_000045.1:n.*7G>T
NM_001146151.3:c.*299G>T (AVPR2) NP_001139623.1:n.*299G>T
NR_027419.2:n.1076G>T (AVPR2)
NM_000054.7:c.*7G>T (AVPR2) MANE Select NP_000045.1:n.*7G>T