Canonical Allele Identifier: CA304854177
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs986059919
gnomAD v4: 19-7528747-C-T
MyVariant Identifiers: chr19:g.7593633C>T (hg19) chr19:g.7528747C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7528747C>T , CM000681.2:g.7528747C>T GRCh38
NC_000019.9:g.7593633C>T , CM000681.1:g.7593633C>T GRCh37
NC_000019.8:g.7499633C>T NCBI36
NG_015806.1:g.11138C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.984+44C>T MANE Select ENSP00000264079.5:n.984+44C>T
ENST00000264079.10:c.984+44C>T ENSP00000264079.5:n.984+44C>T
ENST00000394321.9:n.1299+44C>T
ENST00000595860.5:n.94C>T
NM_020533.2:c.984+44C>T NP_065394.1:n.984+44C>T
NM_020533.3:c.984+44C>T MANE Select NP_065394.1:n.984+44C>T
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