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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:
CA241230225
Gene: LUM
HGNC
NCBI
Linked Data
dbSNP Id:
rs867361338
gnomAD v3:
12-91107223-G-A
gnomAD v4:
12-91107223-G-A
MyVariant Identifiers:
chr12:g.91501000G>A (hg19)
chr12:g.91107223G>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.91107223G>A , CM000674.2:g.91107223G>A
GRCh38
NC_000012.11:g.91501000G>A , CM000674.1:g.91501000G>A
GRCh37
NC_000012.10:g.90025131G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000266718.5:c.862+895C>T
MANE Select
ENSP00000266718.4:n.862+895C>T
ENST00000266718.4:c.862+895C>T
ENSP00000266718.4:n.862+895C>T
ENST00000546642.1:n.612+895C>T
ENST00000548071.1:n.255+895C>T
NM_002345.3:c.862+895C>T
NP_002336.1:n.862+895C>T
NM_002345.4:c.862+895C>T
MANE Select
NP_002336.1:n.862+895C>T
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