Canonical Allele Identifier: CA329528453
Gene: FUNDC1 HGNC NCBI

Linked Data

dbSNP Id: rs189725490
gnomAD v3: X-44540987-A-C
gnomAD v4: X-44540987-A-C
MyVariant Identifiers: chrX:g.44400233A>C (hg19) chrX:g.44540987A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.44540987A>C , CM000685.2:g.44540987A>C GRCh38
NC_000023.10:g.44400233A>C , CM000685.1:g.44400233A>C GRCh37
NC_000023.9:g.44285177A>C NCBI36
NG_021288.1:g.6989T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378045.5:c.185+958T>G MANE Select ENSP00000367284.4:n.185+958T>G
ENST00000378045.4:c.185+958T>G ENSP00000367284.4:n.185+958T>G
ENST00000483115.1:n.360+958T>G
NM_173794.3:c.185+958T>G NP_776155.1:n.185+958T>G
NM_173794.4:c.185+958T>G MANE Select NP_776155.1:n.185+958T>G
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