Canonical Allele Identifier: CA9138885
Gene: MCOLN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1137705
ClinVar RCV Id: RCV001473809 RCV002377807
dbSNP Id: rs758402044
ExAC: 19:7592792 C / T
gnomAD v2: 19-7592792-C-T
gnomAD v4: 19-7527906-C-T
MyVariant Identifiers: chr19:g.7592792C>T (hg19) chr19:g.7527906C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527906C>T , CM000681.2:g.7527906C>T GRCh38
NC_000019.9:g.7592792C>T , CM000681.1:g.7592792C>T GRCh37
NC_000019.8:g.7498792C>T NCBI36
NG_015806.1:g.10297C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.723C>T MANE Select ENSP00000264079.5:p.Asn241=
ENST00000264079.10:c.723C>T ENSP00000264079.5:p.Asn241=
ENST00000394321.9:n.1038C>T
NM_020533.2:c.723C>T NP_065394.1:p.Asn241=
NM_020533.3:c.723C>T MANE Select NP_065394.1:p.Asn241=
Search 100 bp 5'
Search 100 bp 3'