Canonical Allele Identifier: CA884205543
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs1413368398
gnomAD v4: 19-7533280-C-T
MyVariant Identifiers: chr19:g.7598166C>T (hg19) chr19:g.7533280C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533280C>T , CM000681.2:g.7533280C>T GRCh38
NC_000019.9:g.7598166C>T , CM000681.1:g.7598166C>T GRCh37
NC_000019.8:g.7504166C>T NCBI36
NG_013374.1:g.4129C>T
NG_015806.1:g.15671C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.1576-243C>T MANE Select ENSP00000264079.5:n.1576-243C>T
ENST00000264079.10:c.1576-243C>T ENSP00000264079.5:n.1576-243C>T
ENST00000394321.9:n.1891-243C>T
ENST00000599334.1:c.304-243C>T
NM_020533.2:c.1576-243C>T NP_065394.1:n.1576-243C>T
NM_020533.3:c.1576-243C>T MANE Select NP_065394.1:n.1576-243C>T
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