Canonical Allele Identifier: CA23758771
Gene: FOXD3 HGNC NCBI
FOXD3-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs78645479
gnomAD v2: 1-63788302-C-G
gnomAD v3: 1-63322631-C-G
gnomAD v4: 1-63322631-C-G
MyVariant Identifiers: chr1:g.63788302C>G (hg19) chr1:g.63322631C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.63322631C>G , CM000663.2:g.63322631C>G GRCh38
NC_000001.10:g.63788302C>G , CM000663.1:g.63788302C>G GRCh37
NC_000001.9:g.63560890C>G NCBI36
NG_012220.1:g.4573C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371116.4:c.-428C>G (FOXD3) MANE Select ENSP00000360157.2:n.-428C>G
NR_121636.1:n.185+860G>C (FOXD3-AS1)
NR_121637.1:n.88-1168G>C (FOXD3-AS1)
NM_012183.3:c.-428C>G (FOXD3) MANE Select NP_036315.1:n.-428C>G
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