Canonical Allele Identifier: CA631318837
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs1053148031
gnomAD v2: 19-7594848-C-G
gnomAD v3: 19-7529962-C-G
gnomAD v4: 19-7529962-C-G
MyVariant Identifiers: chr19:g.7594848C>G (hg19) chr19:g.7529962C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7529962C>G , CM000681.2:g.7529962C>G GRCh38
NC_000019.9:g.7594848C>G , CM000681.1:g.7594848C>G GRCh37
NC_000019.8:g.7500848C>G NCBI36
NG_013374.1:g.811C>G
NG_015806.1:g.12353C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.1359+250C>G MANE Select ENSP00000264079.5:n.1359+250C>G
ENST00000264079.10:c.1359+250C>G ENSP00000264079.5:n.1359+250C>G
ENST00000394321.9:n.1674+250C>G
ENST00000594692.1:n.355+250C>G
ENST00000595860.5:n.542+250C>G
ENST00000599334.1:c.236+250C>G
NM_020533.2:c.1359+250C>G NP_065394.1:n.1359+250C>G
NM_020533.3:c.1359+250C>G MANE Select NP_065394.1:n.1359+250C>G
Search 100 bp 5'
Search 100 bp 3'