Canonical Allele Identifier: CA2735601087
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs2146022303
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7526354T>C , CM000681.2:g.7526354T>C GRCh38
NC_000019.9:g.7591240T>C , CM000681.1:g.7591240T>C GRCh37
NC_000019.8:g.7497240T>C NCBI36
NG_015806.1:g.8745T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.238-85T>C MANE Select ENSP00000264079.5:n.238-85T>C
ENST00000264079.10:c.238-85T>C ENSP00000264079.5:n.238-85T>C
ENST00000394321.9:n.318-85T>C
ENST00000596008.1:n.115T>C
ENST00000601003.1:c.238-85T>C ENSP00000469074.1:n.238-85T>C
NM_020533.2:c.238-85T>C NP_065394.1:n.238-85T>C
NM_020533.3:c.238-85T>C MANE Select NP_065394.1:n.238-85T>C
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Search 100 bp 3'