Canonical Allele Identifier: CA403084573
Gene: MCOLN1 HGNC NCBI

Linked Data

gnomAD v4: 19-7528188-C-T
MyVariant Identifiers: chr19:g.7593074C>T (hg19) chr19:g.7528188C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7528188C>T , CM000681.2:g.7528188C>T GRCh38
NC_000019.9:g.7593074C>T , CM000681.1:g.7593074C>T GRCh37
NC_000019.8:g.7499074C>T NCBI36
NG_015806.1:g.10579C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.808C>T MANE Select ENSP00000264079.5:p.Arg270Trp
ENST00000264079.10:c.808C>T ENSP00000264079.5:p.Arg270Trp
ENST00000394321.9:n.1123C>T
NM_020533.2:c.808C>T NP_065394.1:p.Arg270Trp
NM_020533.3:c.808C>T MANE Select NP_065394.1:p.Arg270Trp
Search 100 bp 5'
Search 100 bp 3'