Canonical Allele Identifier: CA2576597100
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs2146024632
gnomAD v4: 19-7528728-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7528728T>C , CM000681.2:g.7528728T>C GRCh38
NC_000019.9:g.7593614T>C , CM000681.1:g.7593614T>C GRCh37
NC_000019.8:g.7499614T>C NCBI36
NG_015806.1:g.11119T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.984+25T>C MANE Select ENSP00000264079.5:n.984+25T>C
ENST00000264079.10:c.984+25T>C ENSP00000264079.5:n.984+25T>C
ENST00000394321.9:n.1299+25T>C
ENST00000595860.5:n.75T>C
NM_020533.2:c.984+25T>C NP_065394.1:n.984+25T>C
NM_020533.3:c.984+25T>C MANE Select NP_065394.1:n.984+25T>C
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