Canonical Allele Identifier: CA342057998
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs779659750
gnomAD v2: 1-152281283-C-A
gnomAD v4: 1-152308807-C-A
MyVariant Identifiers: chr1:g.152281283C>A (hg19) chr1:g.152308807C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152308807C>A , CM000663.2:g.152308807C>A GRCh38
NC_000001.10:g.152281283C>A , CM000663.1:g.152281283C>A GRCh37
NC_000001.9:g.150547907C>A NCBI36
NG_016190.1:g.21397G>T , LRG_1028:g.21397G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.6079G>T MANE Select ENSP00000357789.1:p.Ala2027Ser
ENST00000368799.1:c.6079G>T ENSP00000357789.1:p.Ala2027Ser
NM_002016.1:c.6079G>T , LRG_1028t1:c.6079G>T NP_002007.1:p.Ala2027Ser
XM_011509329.1:c.6079G>T XP_011507631.1:p.Ala2027Ser
NM_002016.2:c.6079G>T MANE Select NP_002007.1:p.Ala2027Ser
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