Canonical Allele Identifier: CA2320961751
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs2022567442
gnomAD v4: 19-7526349-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7526349C>T , CM000681.2:g.7526349C>T GRCh38
NC_000019.9:g.7591235C>T , CM000681.1:g.7591235C>T GRCh37
NC_000019.8:g.7497235C>T NCBI36
NG_015806.1:g.8740C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.238-90C>T MANE Select ENSP00000264079.5:n.238-90C>T
ENST00000264079.10:c.238-90C>T ENSP00000264079.5:n.238-90C>T
ENST00000394321.9:n.318-90C>T
ENST00000596008.1:n.110C>T
ENST00000601003.1:c.238-90C>T ENSP00000469074.1:n.238-90C>T
NM_020533.2:c.238-90C>T NP_065394.1:n.238-90C>T
NM_020533.3:c.238-90C>T MANE Select NP_065394.1:n.238-90C>T
Search 100 bp 5'
Search 100 bp 3'