Canonical Allele Identifier: CA9138887
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs201338632
ExAC: 19:7592809 A / G
gnomAD v2: 19-7592809-A-G
gnomAD v3: 19-7527923-A-G
gnomAD v4: 19-7527923-A-G
MyVariant Identifiers: chr19:g.7592809A>G (hg19) chr19:g.7527923A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527923A>G , CM000681.2:g.7527923A>G GRCh38
NC_000019.9:g.7592809A>G , CM000681.1:g.7592809A>G GRCh37
NC_000019.8:g.7498809A>G NCBI36
NG_015806.1:g.10314A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.740A>G MANE Select ENSP00000264079.5:p.Asn247Ser
ENST00000264079.10:c.740A>G ENSP00000264079.5:p.Asn247Ser
ENST00000394321.9:n.1055A>G
NM_020533.2:c.740A>G NP_065394.1:p.Asn247Ser
NM_020533.3:c.740A>G MANE Select NP_065394.1:p.Asn247Ser
Search 100 bp 5'
Search 100 bp 3'