Canonical Allele Identifier: CA344455259
Gene: AVPR1B HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.206224814T>C (hg19) chr1:g.206116517A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206116517A>G , CM000663.2:g.206116517A>G GRCh38
NC_000001.10:g.206224814T>C , CM000663.1:g.206224814T>C GRCh37
NC_000001.9:g.204391437T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000367126.5:c.374T>C MANE Select ENSP00000356094.4:p.Leu125Pro
ENST00000367126.4:c.374T>C ENSP00000356094.4:p.Leu125Pro
ENST00000612906.1:n.36+1147T>C
NM_000707.3:c.374T>C NP_000698.1:p.Leu125Pro
NM_000707.4:c.374T>C NP_000698.1:p.Leu125Pro
NM_000707.5:c.374T>C MANE Select NP_000698.1:p.Leu125Pro
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