Canonical Allele Identifier: CA304853780
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs949465688
MyVariant Identifiers: chr19:g.7592991C>T (hg19) chr19:g.7528105C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7528105C>T , CM000681.2:g.7528105C>T GRCh38
NC_000019.9:g.7592991C>T , CM000681.1:g.7592991C>T GRCh37
NC_000019.8:g.7498991C>T NCBI36
NG_015806.1:g.10496C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.778-53C>T MANE Select ENSP00000264079.5:n.778-53C>T
ENST00000264079.10:c.778-53C>T ENSP00000264079.5:n.778-53C>T
ENST00000394321.9:n.1093-53C>T
NM_020533.2:c.778-53C>T NP_065394.1:n.778-53C>T
NM_020533.3:c.778-53C>T MANE Select NP_065394.1:n.778-53C>T
Search 100 bp 5'
Search 100 bp 3'