Canonical Allele Identifier: CA1233530
Gene: F5 HGNC NCBI

Linked Data

dbSNP Id: rs530654635
ExAC: 1:169498980 A / T
gnomAD v2: 1-169498980-A-T
gnomAD v3: 1-169529742-A-T
MyVariant Identifiers: chr1:g.169498980A>T (hg19) chr1:g.169529742A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169529742A>T , CM000663.2:g.169529742A>T GRCh38
NC_000001.10:g.169498980A>T , CM000663.1:g.169498980A>T GRCh37
NC_000001.9:g.167765604A>T NCBI36
NG_011806.1:g.61790T>A , LRG_553:g.61790T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000367797.9:c.5285T>A MANE Select ENSP00000356771.3:p.Met1762Lys
ENST00000367796.3:c.5300T>A ENSP00000356770.3:p.Met1767Lys
ENST00000367797.7:c.5285T>A ENSP00000356771.3:p.Met1762Lys
NM_000130.4:c.5285T>A , LRG_553t1:c.5285T>A NP_000121.2:p.Met1762Lys
XM_017000660.2:c.4874T>A XP_016856149.1:p.Met1625Lys
NM_000130.5:c.5285T>A MANE Select NP_000121.2:p.Met1762Lys
Search 100 bp 5'
Search 100 bp 3'