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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:
CA384105531
Gene: SLCO1B1
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chr12:g.21331563A>C (hg19)
chr12:g.21178629A>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.21178629A>C , CM000674.2:g.21178629A>C
GRCh38
NC_000012.11:g.21331563A>C , CM000674.1:g.21331563A>C
GRCh37
NC_000012.10:g.21222830A>C
NCBI36
NG_011745.1:g.52436A>C , LRG_1022:g.52436A>C
Transcript Alleles
HGVS
Amino-acid Change
ENST00000256958.3:c.535A>C
MANE Select
ENSP00000256958.2:p.Met179Leu
ENST00000256958.2:c.535A>C
ENSP00000256958.2:p.Met179Leu
NM_006446.4:c.535A>C , LRG_1022t1:c.535A>C
NP_006437.3:p.Met179Leu
NM_006446.5:c.535A>C
MANE Select
NP_006437.3:p.Met179Leu
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