Canonical Allele Identifier: CA1132721982
Gene: FUNDC1 HGNC NCBI

Linked Data

dbSNP Id: rs2038968757
gnomAD v3: X-44540883-T-C
gnomAD v4: X-44540883-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.44540883T>C , CM000685.2:g.44540883T>C GRCh38
NC_000023.10:g.44400129T>C , CM000685.1:g.44400129T>C GRCh37
NC_000023.9:g.44285073T>C NCBI36
NG_021288.1:g.7093A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378045.5:c.185+1062A>G MANE Select ENSP00000367284.4:n.185+1062A>G
ENST00000378045.4:c.185+1062A>G ENSP00000367284.4:n.185+1062A>G
ENST00000483115.1:n.360+1062A>G
NM_173794.3:c.185+1062A>G NP_776155.1:n.185+1062A>G
NM_173794.4:c.185+1062A>G MANE Select NP_776155.1:n.185+1062A>G
Search 100 bp 5'
Search 100 bp 3'