Canonical Allele Identifier: CA2426939913
Gene: FUNDC1 HGNC NCBI

Linked Data

dbSNP Id: rs2038968688

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.44540872G>A , CM000685.2:g.44540872G>A GRCh38
NC_000023.10:g.44400118G>A , CM000685.1:g.44400118G>A GRCh37
NC_000023.9:g.44285062G>A NCBI36
NG_021288.1:g.7104C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378045.5:c.185+1073C>T MANE Select ENSP00000367284.4:n.185+1073C>T
ENST00000378045.4:c.185+1073C>T ENSP00000367284.4:n.185+1073C>T
ENST00000483115.1:n.360+1073C>T
NM_173794.3:c.185+1073C>T NP_776155.1:n.185+1073C>T
NM_173794.4:c.185+1073C>T MANE Select NP_776155.1:n.185+1073C>T