Canonical Allele Identifier: CA342088162
Gene: FLG HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.152284746G>C (hg19) chr1:g.152312270G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152312270G>C , CM000663.2:g.152312270G>C GRCh38
NC_000001.10:g.152284746G>C , CM000663.1:g.152284746G>C GRCh37
NC_000001.9:g.150551370G>C NCBI36
NG_016190.1:g.17934C>G , LRG_1028:g.17934C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.2616C>G MANE Select ENSP00000357789.1:p.Ser872Arg
ENST00000368799.1:c.2616C>G ENSP00000357789.1:p.Ser872Arg
NM_002016.1:c.2616C>G , LRG_1028t1:c.2616C>G NP_002007.1:p.Ser872Arg
XM_011509329.1:c.2616C>G XP_011507631.1:p.Ser872Arg
NM_002016.2:c.2616C>G MANE Select NP_002007.1:p.Ser872Arg
Search 100 bp 5'
Search 100 bp 3'