Canonical Allele Identifier: CA612688703
Community Standard Title: NC_000013.11:g.113105781T>G
Gene: F7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113105781T>G , CM000675.2:g.113105781T>G GRCh38
NC_000013.10:g.113760095T>G , CM000675.1:g.113760095T>G GRCh37
NC_000013.9:g.112808096T>G NCBI36
NG_009262.1:g.4991T>G , LRG_554:g.4991T>G

Transcript Alleles

HGVS Amino-acid Change
XM_006719963.3:c.-16T>G XP_006720026.2:n.-16T>G
XM_011537474.2:c.-16T>G XP_011535776.2:n.-16T>G
XM_011537475.2:c.-16T>G XP_011535777.2:n.-16T>G