Canonical Allele Identifier: CA304853976
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs982178697
MyVariant Identifiers: chr19:g.7593309G>C (hg19) chr19:g.7528423G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7528423G>C , CM000681.2:g.7528423G>C GRCh38
NC_000019.9:g.7593309G>C , CM000681.1:g.7593309G>C GRCh37
NC_000019.8:g.7499309G>C NCBI36
NG_015806.1:g.10814G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.877+166G>C MANE Select ENSP00000264079.5:n.877+166G>C
ENST00000264079.10:c.877+166G>C ENSP00000264079.5:n.877+166G>C
ENST00000394321.9:n.1192+166G>C
NM_020533.2:c.877+166G>C NP_065394.1:n.877+166G>C
NM_020533.3:c.877+166G>C MANE Select NP_065394.1:n.877+166G>C
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