Canonical Allele Identifier: CA884201341
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs1489632500
gnomAD v4: 19-7527790-G-A
MyVariant Identifiers: chr19:g.7592676G>A (hg19) chr19:g.7527790G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527790G>A , CM000681.2:g.7527790G>A GRCh38
NC_000019.9:g.7592676G>A , CM000681.1:g.7592676G>A GRCh37
NC_000019.8:g.7498676G>A NCBI36
NG_015806.1:g.10181G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.681-74G>A MANE Select ENSP00000264079.5:n.681-74G>A
ENST00000264079.10:c.681-74G>A ENSP00000264079.5:n.681-74G>A
ENST00000394321.9:n.922G>A
ENST00000601003.1:c.572-74G>A ENSP00000469074.1:n.572-74G>A
NM_020533.2:c.681-74G>A NP_065394.1:n.681-74G>A
NM_020533.3:c.681-74G>A MANE Select NP_065394.1:n.681-74G>A
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