Canonical Allele Identifier: CA304856697
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs183358355
MyVariant Identifiers: chr19:g.7598074C>A (hg19) chr19:g.7533188C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533188C>A , CM000681.2:g.7533188C>A GRCh38
NC_000019.9:g.7598074C>A , CM000681.1:g.7598074C>A GRCh37
NC_000019.8:g.7504074C>A NCBI36
NG_013374.1:g.4037C>A
NG_015806.1:g.15579C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.1576-335C>A MANE Select ENSP00000264079.5:n.1576-335C>A
ENST00000264079.10:c.1576-335C>A ENSP00000264079.5:n.1576-335C>A
ENST00000394321.9:n.1891-335C>A
ENST00000599334.1:c.304-335C>A
NM_020533.2:c.1576-335C>A NP_065394.1:n.1576-335C>A
NM_020533.3:c.1576-335C>A MANE Select NP_065394.1:n.1576-335C>A
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