LDH info

Canonical Allele Identifier: CA15532051
Gene: FOXP2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs6466479

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.114101050T>G , CM000669.2:g.114101050T>G GRCh38
NC_000007.13:g.113741105T>G , CM000669.1:g.113741105T>G GRCh37
NC_000007.12:g.113528341T>G NCBI36
NG_007491.2:g.19741T>G
NG_007491.3:g.19741T>G

Transcript Alleles

HGVS Amino-acid change
NR_033766.1:n.302+14439T>G
XM_011516706.1:c.-360+14439T>G XP_011515008.1:p.=
XM_017012801.2:c.-247+12622T>G XP_016868290.1:p.=
NR_033766.2:n.285+14439T>G
ENST00000412402.5:c.-102+14439T>G ENSP00000405470.1:p.=
ENST00000440349.5:c.-247+14439T>G ENSP00000395552.1:p.=
ENST00000441290.6:c.-435+14439T>G ENSP00000416825.1:p.=
ENST00000495516.1:n.105+12780T>G
ENST00000635638.1:c.-247+13212T>G ENSP00000489073.1:p.=