Canonical Allele Identifier: CA631462880
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs1327347051
gnomAD v2: 19-7598694-G-A
gnomAD v4: 19-7533808-G-A
MyVariant Identifiers: chr19:g.7598694G>A (hg19) chr19:g.7533808G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533808G>A , CM000681.2:g.7533808G>A GRCh38
NC_000019.9:g.7598694G>A , CM000681.1:g.7598694G>A GRCh37
NC_000019.8:g.7504694G>A NCBI36
NG_013374.1:g.4657G>A
NG_015806.1:g.16199G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.*13G>A MANE Select ENSP00000264079.5:n.*13G>A
ENST00000264079.10:c.*13G>A ENSP00000264079.5:n.*13G>A
ENST00000394321.9:n.2071G>A
ENST00000599334.1:c.484G>A
ENST00000601870.1:c.109G>A
ENST00000602227.1:n.310G>A
NM_020533.2:c.*13G>A NP_065394.1:n.*13G>A
NM_020533.3:c.*13G>A MANE Select NP_065394.1:n.*13G>A
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