Canonical Allele Identifier: CA10788261
Gene: AVPR1B HGNC NCBI

Linked Data

dbSNP Id: rs33933482
gnomAD v2: 1-206231264-G-A
gnomAD v3: 1-206110067-C-T
gnomAD v4: 1-206110067-C-T
MyVariant Identifiers: chr1:g.206231264G>A (hg19) chr1:g.206110067C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206110067C>T , CM000663.2:g.206110067C>T GRCh38
NC_000001.10:g.206231264G>A , CM000663.1:g.206231264G>A GRCh37
NC_000001.9:g.204397887G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000367126.5:c.*122G>A MANE Select ENSP00000356094.4:n.*122G>A
ENST00000367126.4:c.*122G>A ENSP00000356094.4:n.*122G>A
ENST00000612906.1:n.493G>A
NM_000707.3:c.*122G>A NP_000698.1:n.*122G>A
NM_000707.4:c.*122G>A NP_000698.1:n.*122G>A
NM_000707.5:c.*122G>A MANE Select NP_000698.1:n.*122G>A
Search 100 bp 5'
Search 100 bp 3'