Canonical Allele Identifier: CA350073548

Gene: FASTKD2

Linked Data

• dbSNP Id: rs1689553743
• gnomAD v3: 2-206767470-G-C
• gnomAD v4: 2-206767470-G-C
• MyVariant Identifiers: chr2:g.207632194G>C (hg19) ; chr2:g.206767470G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206767470G>C , CM000664.2:g.206767470G>C	GRCh38
NC_000002.11:g.207632194G>C , CM000664.1:g.207632194G>C	GRCh37
NC_000002.10:g.207340439G>C	NCBI36
NG_008984.1:g.7083G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402774.8:c.777G>C MANE Select	ENSP00000385990.3:p.Gln259His
ENST00000236980.10:c.777G>C	ENSP00000236980.6:p.Gln259His
ENST00000402774.7:c.777G>C	ENSP00000385990.3:p.Gln259His
ENST00000403094.3:c.777G>C	ENSP00000384929.3:p.Gln259His
ENST00000487777.5:n.835G>C
NM_001136193.1:c.777G>C	NP_001129665.1:p.Gln259His
NM_001136194.1:c.777G>C	NP_001129666.1:p.Gln259His
NM_014929.3:c.777G>C	NP_055744.2:p.Gln259His
NM_001136193.2:c.777G>C MANE Select	NP_001129665.1:p.Gln259His
NM_001136194.2:c.777G>C	NP_001129666.1:p.Gln259His
NM_014929.4:c.777G>C	NP_055744.2:p.Gln259His