Canonical Allele Identifier: CA280620
Gene: MEFV HGNC NCBI

Linked Data

ClinVar Variation Id: 97529
ClinVar RCV Id: RCV000083781
dbSNP Id: rs104895125

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3254532C>A , CM000678.2:g.3254532C>A GRCh38
NC_000016.9:g.3304532C>A , CM000678.1:g.3304532C>A GRCh37
NC_000016.8:g.3244533C>A NCBI36
NG_007871.1:g.7096G>T , LRG_190:g.7096G>T

Transcript Alleles

HGVS Amino-acid change
NM_000243.2:c.536G>T , LRG_190t1:c.536G>T NP_000234.1:p.Ser179Ile
NM_001198536.1:c.277+1779G>T NP_001185465.1:p.=
XM_017023236.2:c.536G>T XP_016878725.1:p.Ser179Ile
XR_001751903.1:n.725G>T
NM_000243.3:c.536G>T MANE Select NP_000234.1:p.Ser179Ile
NM_001198536.2:c.277+1779G>T NP_001185465.2:p.=
ENST00000219596.5:c.536G>T ENSP00000219596.1:p.Ser179Ile
ENST00000339854.8:c.277+1779G>T ENSP00000339639.4:p.=
ENST00000536379.5:n.277+1779G>T ENSP00000445079.1:p.=
ENST00000536980.5:c.277+1779G>T ENSP00000444178.1:p.=
ENST00000537682.5:c.536G>T ENSP00000438611.1:p.Ser179Ile
ENST00000538326.5:c.536G>T ENSP00000437486.1:p.Ser179Ile
ENST00000539145.5:n.277+1779G>T ENSP00000444471.1:p.=
ENST00000541159.5:n.277+1779G>T ENSP00000438711.1:p.=
ENST00000542898.5:c.536G>T ENSP00000444615.1:p.Ser179Ile
ENST00000570511.5:n.536G>T ENSP00000458312.1:p.Ser179Ile
ENST00000572244.5:n.277+1779G>T ENSP00000461186.1:p.=
ENST00000574583.5:n.277+1779G>T ENSP00000460269.1:p.=
ENST00000576315.5:n.277+1779G>T ENSP00000460551.1:p.=
ENST00000621655.1:n.277+1779G>T ENSP00000481436.1:p.=