Canonical Allele Identifier: CA1137751301

Gene: F9

Linked Data

• dbSNP Id: rs1265586158
• gnomAD v3: X-139562195-T-C
• gnomAD v4: X-139562195-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139562195T>C , CM000685.2:g.139562195T>C	GRCh38
NC_000023.10:g.138644354T>C , CM000685.1:g.138644354T>C	GRCh37
NC_000023.9:g.138472020T>C	NCBI36
NG_007994.1:g.36460T>C , LRG_556:g.36460T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.*124T>C MANE Select	ENSP00000218099.2:n.*124T>C
ENST00000643157.1:n.1723+454T>C
ENST00000218099.6:c.*124T>C	ENSP00000218099.2:n.*124T>C
NM_000133.3:c.*124T>C , LRG_556t1:c.*124T>C	NP_000124.1:n.*124T>C
NM_001313913.1:c.*124T>C	NP_001300842.1:n.*124T>C
XM_005262397.3:c.*124T>C	XP_005262454.1:n.*124T>C
XM_005262397.4:c.*124T>C	XP_005262454.1:n.*124T>C
NM_000133.4:c.*124T>C MANE Select	NP_000124.1:n.*124T>C
NM_001313913.2:c.*124T>C	NP_001300842.1:n.*124T>C