Canonical Allele Identifier: CA304853764
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs990966092
gnomAD v2: 19-7592967-C-T
gnomAD v3: 19-7528081-C-T
gnomAD v4: 19-7528081-C-T
MyVariant Identifiers: chr19:g.7592967C>T (hg19) chr19:g.7528081C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7528081C>T , CM000681.2:g.7528081C>T GRCh38
NC_000019.9:g.7592967C>T , CM000681.1:g.7592967C>T GRCh37
NC_000019.8:g.7498967C>T NCBI36
NG_015806.1:g.10472C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.778-77C>T MANE Select ENSP00000264079.5:n.778-77C>T
ENST00000264079.10:c.778-77C>T ENSP00000264079.5:n.778-77C>T
ENST00000394321.9:n.1093-77C>T
NM_020533.2:c.778-77C>T NP_065394.1:n.778-77C>T
NM_020533.3:c.778-77C>T MANE Select NP_065394.1:n.778-77C>T
Search 100 bp 5'
Search 100 bp 3'