Canonical Allele Identifier: CA1206156995
Gene: F5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169586588_169586589delinsTG , CM000663.2:g.169586588_169586589delinsTG GRCh38
NC_000001.10:g.169555826_169555827delinsTG , CM000663.1:g.169555826_169555827delinsTG GRCh37
NC_000001.9:g.167822450_167822451delinsTG NCBI36
NG_011806.1:g.4943_4944delinsCA , LRG_553:g.4943_4944delinsCA

Transcript Alleles

HGVS Amino-acid Change
XM_017000660.2:c.-522_-521delinsCA XP_016856149.1:n.-522_-521delinsCA