Canonical Allele Identifier: CA884201944
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs548834197
gnomAD v3: 19-7528400-C-G
gnomAD v4: 19-7528400-C-G
MyVariant Identifiers: chr19:g.7593286C>G (hg19) chr19:g.7528400C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7528400C>G , CM000681.2:g.7528400C>G GRCh38
NC_000019.9:g.7593286C>G , CM000681.1:g.7593286C>G GRCh37
NC_000019.8:g.7499286C>G NCBI36
NG_015806.1:g.10791C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.877+143C>G MANE Select ENSP00000264079.5:n.877+143C>G
ENST00000264079.10:c.877+143C>G ENSP00000264079.5:n.877+143C>G
ENST00000394321.9:n.1192+143C>G
NM_020533.2:c.877+143C>G NP_065394.1:n.877+143C>G
NM_020533.3:c.877+143C>G MANE Select NP_065394.1:n.877+143C>G
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