Canonical Allele Identifier: CA631462902
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs760469616
gnomAD v2: 19-7598731-G-T
gnomAD v3: 19-7533845-G-T
gnomAD v4: 19-7533845-G-T
MyVariant Identifiers: chr19:g.7598731G>T (hg19) chr19:g.7598731_7598732delinsTC (hg19) chr19:g.7533845G>T (hg38) chr19:g.7533845_7533846delinsTC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533845G>T , CM000681.2:g.7533845G>T GRCh38
NC_000019.9:g.7598731G>T , CM000681.1:g.7598731G>T GRCh37
NC_000019.8:g.7504731G>T NCBI36
NG_013374.1:g.4694G>T
NG_015806.1:g.16236G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.*50G>T MANE Select ENSP00000264079.5:n.*50G>T
ENST00000264079.10:c.*50G>T ENSP00000264079.5:n.*50G>T
ENST00000394321.9:n.2108G>T
ENST00000599334.1:c.521G>T
ENST00000601870.1:c.146G>T
ENST00000602227.1:n.347G>T
NM_020533.2:c.*50G>T NP_065394.1:n.*50G>T
NM_020533.3:c.*50G>T MANE Select NP_065394.1:n.*50G>T
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Search 100 bp 3'