Canonical Allele Identifier: CA304856704
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs1042394532
MyVariant Identifiers: chr19:g.7598075C>G (hg19) chr19:g.7533189C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533189C>G , CM000681.2:g.7533189C>G GRCh38
NC_000019.9:g.7598075C>G , CM000681.1:g.7598075C>G GRCh37
NC_000019.8:g.7504075C>G NCBI36
NG_013374.1:g.4038C>G
NG_015806.1:g.15580C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.1576-334C>G MANE Select ENSP00000264079.5:n.1576-334C>G
ENST00000264079.10:c.1576-334C>G ENSP00000264079.5:n.1576-334C>G
ENST00000394321.9:n.1891-334C>G
ENST00000599334.1:c.304-334C>G
NM_020533.2:c.1576-334C>G NP_065394.1:n.1576-334C>G
NM_020533.3:c.1576-334C>G MANE Select NP_065394.1:n.1576-334C>G
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