Canonical Allele Identifier: CA884205429
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs1163966803
MyVariant Identifiers: chr19:g.7597979A>G (hg19) chr19:g.7533093A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533093A>G , CM000681.2:g.7533093A>G GRCh38
NC_000019.9:g.7597979A>G , CM000681.1:g.7597979A>G GRCh37
NC_000019.8:g.7503979A>G NCBI36
NG_013374.1:g.3942A>G
NG_015806.1:g.15484A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.1576-430A>G MANE Select ENSP00000264079.5:n.1576-430A>G
ENST00000264079.10:c.1576-430A>G ENSP00000264079.5:n.1576-430A>G
ENST00000394321.9:n.1891-430A>G
ENST00000599334.1:c.304-430A>G
NM_020533.2:c.1576-430A>G NP_065394.1:n.1576-430A>G
NM_020533.3:c.1576-430A>G MANE Select NP_065394.1:n.1576-430A>G
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