Canonical Allele Identifier: CA884201257
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs776933291
gnomAD v3: 19-7527701-A-C
gnomAD v4: 19-7527701-A-C
MyVariant Identifiers: chr19:g.7592587A>C (hg19) chr19:g.7527701A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527701A>C , CM000681.2:g.7527701A>C GRCh38
NC_000019.9:g.7592587A>C , CM000681.1:g.7592587A>C GRCh37
NC_000019.8:g.7498587A>C NCBI36
NG_015806.1:g.10092A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.680+73A>C MANE Select ENSP00000264079.5:n.680+73A>C
ENST00000264079.10:c.680+73A>C ENSP00000264079.5:n.680+73A>C
ENST00000394321.9:n.833A>C
ENST00000598406.1:n.574A>C
ENST00000601003.1:c.572-163A>C ENSP00000469074.1:n.572-163A>C
NM_020533.2:c.680+73A>C NP_065394.1:n.680+73A>C
NM_020533.3:c.680+73A>C MANE Select NP_065394.1:n.680+73A>C
Search 100 bp 5'
Search 100 bp 3'