Canonical Allele Identifier: CA12361664
Gene: RNASET2 HGNC NCBI

Linked Data

dbSNP Id: rs9459805
gnomAD v2: 6-167336151-A-G
gnomAD v3: 6-166922663-A-G
gnomAD v4: 6-166922663-A-G
MyVariant Identifiers: chr6:g.167336151A>G (hg19) chr6:g.166922663A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.166922663A>G , CM000668.2:g.166922663A>G GRCh38
NC_000006.11:g.167336151A>G , CM000668.1:g.167336151A>G GRCh37
NC_000006.10:g.167256141A>G NCBI36
NG_016280.2:g.38927T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000508775.6:c.*6925T>C MANE Select ENSP00000426455.2:n.*6925T>C
ENST00000507747.1:c.434+11428T>C
NM_003730.5:c.*6925T>C NP_003721.2:n.*6925T>C
NM_003730.6:c.*6925T>C MANE Select NP_003721.2:n.*6925T>C
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