Canonical Allele Identifier: CA641658899
Gene: FUNDC1 HGNC NCBI

Linked Data

dbSNP Id: rs1245127114
gnomAD v2: X-44400288-C-A
gnomAD v3: X-44541042-C-A
gnomAD v4: X-44541042-C-A
MyVariant Identifiers: chrX:g.44400288C>A (hg19) chrX:g.44541042C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.44541042C>A , CM000685.2:g.44541042C>A GRCh38
NC_000023.10:g.44400288C>A , CM000685.1:g.44400288C>A GRCh37
NC_000023.9:g.44285232C>A NCBI36
NG_021288.1:g.6934G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378045.5:c.185+903G>T MANE Select ENSP00000367284.4:n.185+903G>T
ENST00000378045.4:c.185+903G>T ENSP00000367284.4:n.185+903G>T
ENST00000483115.1:n.360+903G>T
NM_173794.3:c.185+903G>T NP_776155.1:n.185+903G>T
NM_173794.4:c.185+903G>T MANE Select NP_776155.1:n.185+903G>T
Search 100 bp 5'
Search 100 bp 3'