Canonical Allele Identifier: CA431115241
Gene: FASTKD2 HGNC NCBI

Linked Data

dbSNP Id: rs759342298
MyVariant Identifiers: chr2:g.207631864A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.206767140A>C , CM000664.2:g.206767140A>C GRCh38
NC_000002.11:g.207631864A>C , CM000664.1:g.207631864A>C GRCh37
NC_000002.10:g.207340109A>C NCBI36
NG_008984.1:g.6753A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000402774.8:c.447A>C MANE Select ENSP00000385990.3:p.Thr149=
ENST00000236980.10:c.447A>C ENSP00000236980.6:p.Thr149=
ENST00000402774.7:c.447A>C ENSP00000385990.3:p.Thr149=
ENST00000403094.3:c.447A>C ENSP00000384929.3:p.Thr149=
ENST00000487777.5:n.505A>C
NM_001136193.1:c.447A>C NP_001129665.1:p.Thr149=
NM_001136194.1:c.447A>C NP_001129666.1:p.Thr149=
NM_014929.3:c.447A>C NP_055744.2:p.Thr149=
NM_001136193.2:c.447A>C MANE Select NP_001129665.1:p.Thr149=
NM_001136194.2:c.447A>C NP_001129666.1:p.Thr149=
NM_014929.4:c.447A>C NP_055744.2:p.Thr149=