Canonical Allele Identifier: CA884200606
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs1183859371
gnomAD v3: 19-7527183-G-T
gnomAD v4: 19-7527183-G-T
MyVariant Identifiers: chr19:g.7592069G>T (hg19) chr19:g.7527183G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7527183G>T , CM000681.2:g.7527183G>T GRCh38
NC_000019.9:g.7592069G>T , CM000681.1:g.7592069G>T GRCh37
NC_000019.8:g.7498069G>T NCBI36
NG_015806.1:g.9574G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.571+257G>T MANE Select ENSP00000264079.5:n.571+257G>T
ENST00000264079.10:c.571+257G>T ENSP00000264079.5:n.571+257G>T
ENST00000394321.9:n.651+257G>T
ENST00000598406.1:n.392+257G>T
ENST00000601003.1:c.571+257G>T ENSP00000469074.1:n.571+257G>T
NM_020533.2:c.571+257G>T NP_065394.1:n.571+257G>T
NM_020533.3:c.571+257G>T MANE Select NP_065394.1:n.571+257G>T
Search 100 bp 5'
Search 100 bp 3'