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UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
CA402583957
Gene: RAX
HGNC
NCBI
Linked Data
dbSNP Id:
rs2070309493
gnomAD v4:
18-59269140-G-C
MyVariant Identifiers:
chr18:g.56936372G>C (hg19)
chr18:g.59269140G>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.59269140G>C , CM000680.2:g.59269140G>C
GRCh38
NC_000018.9:g.56936372G>C , CM000680.1:g.56936372G>C
GRCh37
NC_000018.8:g.55087352G>C
NCBI36
NG_013031.1:g.9254C>G
Transcript Alleles
HGVS
Amino-acid change
ENST00000334889.4:c.905C>G
MANE Select
ENSP00000334813.3:p.Ser302Cys
ENST00000256852.7:c.*336C>G
ENSP00000256852.7:n.*336C>G
ENST00000334889.3:c.905C>G
ENSP00000334813.3:p.Ser302Cys
NM_013435.2:c.905C>G
NP_038463.2:p.Ser302Cys
NM_013435.3:c.905C>G
MANE Select
NP_038463.2:p.Ser302Cys
Search 100 bp 5'
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