Canonical Allele Identifier: CA2320962628
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs2022597976
gnomAD v4: 19-7528056-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7528056G>A , CM000681.2:g.7528056G>A GRCh38
NC_000019.9:g.7592942G>A , CM000681.1:g.7592942G>A GRCh37
NC_000019.8:g.7498942G>A NCBI36
NG_015806.1:g.10447G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.777+96G>A MANE Select ENSP00000264079.5:n.777+96G>A
ENST00000264079.10:c.777+96G>A ENSP00000264079.5:n.777+96G>A
ENST00000394321.9:n.1092+96G>A
NM_020533.2:c.777+96G>A NP_065394.1:n.777+96G>A
NM_020533.3:c.777+96G>A MANE Select NP_065394.1:n.777+96G>A
Search 100 bp 5'
Search 100 bp 3'