Canonical Allele Identifier: CA276954780

Gene: MEFV

Linked Data

• dbSNP Id: rs991883184
• gnomAD v2: 16-3292969-T-A
• gnomAD v3: 16-3242969-T-A
• gnomAD v4: 16-3242969-T-A
• MyVariant Identifiers: chr16:g.3292969T>A (hg19) ; chr16:g.3242969T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3242969T>A , CM000678.2:g.3242969T>A	GRCh38
NC_000016.9:g.3292969T>A , CM000678.1:g.3292969T>A	GRCh37
NC_000016.8:g.3232970T>A	NCBI36
NG_007871.1:g.18659A>T , LRG_190:g.18659A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697124.1:n.1639A>T
ENST00000219596.6:c.*172A>T MANE Select	ENSP00000219596.1:n.*172A>T
ENST00000219596.5:c.*172A>T	ENSP00000219596.1:n.*172A>T
ENST00000339854.8:c.*172A>T	ENSP00000339639.4:n.*172A>T
ENST00000536980.5:c.*794A>T	ENSP00000444178.1:n.*794A>T
ENST00000537682.5:c.*794A>T	ENSP00000438611.1:n.*794A>T
ENST00000538326.5:c.*1143A>T	ENSP00000437486.1:n.*1143A>T
ENST00000542898.5:c.*794A>T	ENSP00000444615.1:n.*794A>T
NM_000243.2:c.*172A>T , LRG_190t1:c.*172A>T	NP_000234.1:n.*172A>T
NM_001198536.1:c.*722A>T	NP_001185465.1:n.*722A>T
NM_000243.3:c.*172A>T MANE Select	NP_000234.1:n.*172A>T
NM_001198536.2:c.*722A>T	NP_001185465.2:n.*722A>T