Canonical Allele Identifier: CA4289917
Gene: DNAJC30 HGNC NCBI

Linked Data

dbSNP Id: rs782609560
ExAC: 7:73097314 G / A
gnomAD v2: 7-73097314-G-A
gnomAD v3: 7-73682984-G-A
gnomAD v4: 7-73682984-G-A
MyVariant Identifiers: chr7:g.73097314G>A (hg19) chr7:g.73682984G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.73682984G>A , CM000669.2:g.73682984G>A GRCh38
NC_000007.13:g.73097314G>A , CM000669.1:g.73097314G>A GRCh37
NC_000007.12:g.72735250G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000395176.3:c.440C>T MANE Select ENSP00000378605.1:p.Thr147Ile
ENST00000395176.2:c.440C>T ENSP00000378605.1:p.Thr147Ile
NM_032317.2:c.440C>T NP_115693.2:p.Thr147Ile
NM_032317.3:c.440C>T MANE Select NP_115693.2:p.Thr147Ile
Search 100 bp 5'
Search 100 bp 3'