Canonical Allele Identifier: CA3209264
Gene: ANKH HGNC NCBI

Linked Data

ClinVar Variation Id: 281904
ClinVar RCV Id: RCV000399069
dbSNP Id: rs199583793
ExAC: 5:14871530 G / A
gnomAD v2: 5-14871530-G-A
gnomAD v3: 5-14871421-G-A
gnomAD v4: 5-14871421-G-A
MyVariant Identifiers: chr5:g.14871530G>A (hg19) chr5:g.14871421G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14871421G>A , CM000667.2:g.14871421G>A GRCh38
NC_000005.9:g.14871530G>A , CM000667.1:g.14871530G>A GRCh37
NC_000005.8:g.14924530G>A NCBI36
NG_008273.1:g.5358C>T
NG_008273.2:g.5365C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.27C>T MANE Select ENSP00000284268.6:p.His9=
ENST00000284268.6:c.27C>T ENSP00000284268.6:p.His9=
ENST00000505140.1:c.27C>T ENSP00000426332.1:p.His9=
ENST00000513115.1:n.52C>T
NM_054027.4:c.27C>T NP_473368.1:p.His9=
XM_011514067.1:c.27C>T XP_011512369.1:p.His9=
NM_054027.5:c.27C>T NP_473368.1:p.His9=
NM_054027.6:c.27C>T MANE Select NP_473368.1:p.His9=
Search 100 bp 5'
Search 100 bp 3'