Canonical Allele Identifier: CA2426939947
Gene: FUNDC1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.44540984C= , CM000685.2:g.44540984C= GRCh38
NC_000023.10:g.44400230C= , CM000685.1:g.44400230C= GRCh37
NC_000023.9:g.44285174C= NCBI36
NG_021288.1:g.6992G=

Transcript Alleles

HGVS Amino-acid change
ENST00000378045.5:c.185+961G= MANE Select ENSP00000367284.4:n.185+961G=
ENST00000378045.4:c.185+961G= ENSP00000367284.4:n.185+961G=
ENST00000483115.1:n.360+961G=
NM_173794.3:c.185+961G= NP_776155.1:n.185+961G=
NM_173794.4:c.185+961G= MANE Select NP_776155.1:n.185+961G=
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