Canonical Allele Identifier: CA304855026
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs879245291
MyVariant Identifiers: chr19:g.7595115A>C (hg19) chr19:g.7530229A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7530229A>C , CM000681.2:g.7530229A>C GRCh38
NC_000019.9:g.7595115A>C , CM000681.1:g.7595115A>C GRCh37
NC_000019.8:g.7501115A>C NCBI36
NG_013374.1:g.1078A>C
NG_015806.1:g.12620A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264079.11:c.1360-57A>C MANE Select ENSP00000264079.5:n.1360-57A>C
ENST00000264079.10:c.1360-57A>C ENSP00000264079.5:n.1360-57A>C
ENST00000394321.9:n.1675-57A>C
ENST00000594692.1:n.356-57A>C
ENST00000595860.5:n.543-57A>C
ENST00000599334.1:c.237-206A>C
NM_020533.2:c.1360-57A>C NP_065394.1:n.1360-57A>C
NM_020533.3:c.1360-57A>C MANE Select NP_065394.1:n.1360-57A>C
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