Canonical Allele Identifier: CA875592734
Gene: FUNDC1 HGNC NCBI

Linked Data

dbSNP Id: rs1194842675
MyVariant Identifiers: chrX:g.44400230C>G (hg19) chrX:g.44540984C>G (hg38)
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Genomic Alleles

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

Transcript Alleles

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