Canonical Allele Identifier: CA916081980
Community Standard Title: NC_000023.11:g.139530731A>G
Gene: F9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139530731A>G , CM000685.2:g.139530731A>G GRCh38
NC_000023.10:g.138612890A>G , CM000685.1:g.138612890A>G GRCh37
NC_000023.9:g.138440556A>G NCBI36
NG_007994.1:g.4996A>G , LRG_556:g.4996A>G

Transcript Alleles

HGVS Amino-acid Change
XM_005262397.4:c.-34A>G XP_005262454.1:n.-34A>G