Canonical Allele Identifier: CA631319451
Gene: MCOLN1 HGNC NCBI

Linked Data

dbSNP Id: rs1485986128
gnomAD v2: 19-7598825-T-G
gnomAD v3: 19-7533939-T-G
gnomAD v4: 19-7533939-T-G
MyVariant Identifiers: chr19:g.7598825T>G (hg19) chr19:g.7533939T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7533939T>G , CM000681.2:g.7533939T>G GRCh38
NC_000019.9:g.7598825T>G , CM000681.1:g.7598825T>G GRCh37
NC_000019.8:g.7504825T>G NCBI36
NG_013374.1:g.4788T>G
NG_015806.1:g.16330T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.*144T>G MANE Select ENSP00000264079.5:n.*144T>G
ENST00000264079.10:c.*144T>G ENSP00000264079.5:n.*144T>G
ENST00000394321.9:n.2202T>G
ENST00000599334.1:c.615T>G
ENST00000601870.1:c.169+71T>G
ENST00000602227.1:n.441T>G
NM_020533.2:c.*144T>G NP_065394.1:n.*144T>G
NM_020533.3:c.*144T>G MANE Select NP_065394.1:n.*144T>G
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