Canonical Allele Identifier: CA295269960

Gene: FN3KRP

Linked Data

• dbSNP Id: rs975640003
• MyVariant Identifiers: chr17:g.80685814C>T (hg19) ; chr17:g.82727938C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727938C>T , CM000679.2:g.82727938C>T	GRCh38
NC_000017.10:g.80685814C>T , CM000679.1:g.80685814C>T	GRCh37
NC_000017.9:g.78279103C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*767C>T MANE Select	ENSP00000269373.6:n.*767C>T
ENST00000269373.10:c.*767C>T	ENSP00000269373.6:n.*767C>T
ENST00000571594.1:c.53+771C>T	ENSP00000459751.1:n.53+771C>T
NM_024619.3:c.*767C>T	NP_078895.2:n.*767C>T
NR_046408.1:n.1875C>T
XM_024450948.1:c.*767C>T	XP_024306716.1:n.*767C>T
NM_024619.4:c.*767C>T MANE Select	NP_078895.2:n.*767C>T
NR_046408.2:n.1875C>T