Canonical Allele Identifier: CA153691887
Gene: FOXK1 HGNC NCBI

Linked Data

dbSNP Id: rs9791644
MyVariant Identifiers: chr7:g.4683903G>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.4683903G>C , CM000669.2:g.4683903G>C GRCh38
NC_000007.13:g.4723534G>C , CM000669.1:g.4723534G>C GRCh37
NC_000007.12:g.4690060G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000328914.5:c.560+1035G>C MANE Select ENSP00000328720.4:n.560+1035G>C
ENST00000328914.4:c.560+1035G>C ENSP00000328720.4:n.560+1035G>C
NM_001037165.1:c.560+1035G>C NP_001032242.1:n.560+1035G>C
XM_011515191.1:c.71+8578G>C XP_011513493.1:n.71+8578G>C
XM_011515191.3:c.71+8578G>C XP_011513493.1:n.71+8578G>C
XM_024446685.1:c.71+8578G>C XP_024302453.1:n.71+8578G>C
NM_001037165.2:c.560+1035G>C MANE Select NP_001032242.1:n.560+1035G>C