Canonical Allele Identifier: CA32405988
Gene: F5 HGNC NCBI

Linked Data

dbSNP Id: rs192909481
gnomAD v2: 1-169541782-G-A
gnomAD v3: 1-169572544-G-A
gnomAD v4: 1-169572544-G-A
MyVariant Identifiers: chr1:g.169541782G>A (hg19) chr1:g.169572544G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169572544G>A , CM000663.2:g.169572544G>A GRCh38
NC_000001.10:g.169541782G>A , CM000663.1:g.169541782G>A GRCh37
NC_000001.9:g.167808406G>A NCBI36
NG_011806.1:g.18988C>T , LRG_553:g.18988C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.251-201C>T MANE Select ENSP00000356771.3:n.251-201C>T
ENST00000367796.3:c.251-201C>T ENSP00000356770.3:n.251-201C>T
ENST00000367797.7:c.251-201C>T ENSP00000356771.3:n.251-201C>T
NM_000130.4:c.251-201C>T , LRG_553t1:c.251-201C>T NP_000121.2:n.251-201C>T
XM_017000660.2:c.-161-201C>T XP_016856149.1:n.-161-201C>T
NM_000130.5:c.251-201C>T MANE Select NP_000121.2:n.251-201C>T
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