Canonical Allele Identifier: CA403083888
Gene: MCOLN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.7592775C>G (hg19) chr19:g.7527889C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527889C>G , CM000681.2:g.7527889C>G GRCh38
NC_000019.9:g.7592775C>G , CM000681.1:g.7592775C>G GRCh37
NC_000019.8:g.7498775C>G NCBI36
NG_015806.1:g.10280C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.706C>G MANE Select ENSP00000264079.5:p.Arg236Gly
ENST00000264079.10:c.706C>G ENSP00000264079.5:p.Arg236Gly
ENST00000394321.9:n.1021C>G
ENST00000601003.1:c.597C>G ENSP00000469074.1:p.Ser199=
NM_020533.2:c.706C>G NP_065394.1:p.Arg236Gly
NM_020533.3:c.706C>G MANE Select NP_065394.1:p.Arg236Gly
Search 100 bp 5'
Search 100 bp 3'