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Canonical Allele Identifier:
CA15341549
Gene: LINC00504
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.14812027A>G
GRCh37
chr4:g.14813651A>G
Linked Data - Sequence & Population
gnomAD v2:
4:14813651 A / G
gnomAD v3:
4:14812027 A / G
gnomAD v4:
chr4-14812027-A-G
Joint Max Group AF
0.30358028 (SAS)
Genomes Max Group AF
0.30358028 (SAS)
Linked Data - NCBI & NCI
dbSNP:
6811874
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.14812027A>G , CM000666.2:g.14812027A>G
GRCh38
NC_000004.11:g.14813651A>G , CM000666.1:g.14813651A>G
GRCh37
NC_000004.10:g.14422749A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_126435.1:n.185+47516T>C
Search 100 bp 5'
Search 100 bp 3'