Canonical Allele Identifier: CA2482862229
Gene: AVPR1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206116509T= , CM000663.2:g.206116509T= GRCh38
NC_000001.10:g.206224822A= , CM000663.1:g.206224822A= GRCh37
NC_000001.9:g.204391445A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000367126.5:c.382A= MANE Select ENSP00000356094.4:p.Met128=
ENST00000367126.4:c.382A= ENSP00000356094.4:p.Met128=
ENST00000612906.1:n.36+1155A=
NM_000707.3:c.382A= NP_000698.1:p.Met128=
NM_000707.4:c.382A= NP_000698.1:p.Met128=
NM_000707.5:c.382A= MANE Select NP_000698.1:p.Met128=