Canonical Allele Identifier: CA1073473797
Gene: ANKH HGNC NCBI

Linked Data

dbSNP Id: rs1735829365
gnomAD v3: 5-14871553-G-A
gnomAD v4: 5-14871553-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14871553G>A , CM000667.2:g.14871553G>A GRCh38
NC_000005.9:g.14871662G>A , CM000667.1:g.14871662G>A GRCh37
NC_000005.8:g.14924662G>A NCBI36
NG_008273.1:g.5226C>T
NG_008273.2:g.5233C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.-106C>T MANE Select ENSP00000284268.6:n.-106C>T
ENST00000284268.6:c.-106C>T ENSP00000284268.6:n.-106C>T
ENST00000505140.1:c.-106C>T ENSP00000426332.1:n.-106C>T
NM_054027.4:c.-106C>T NP_473368.1:n.-106C>T
XM_011514067.1:c.-106C>T XP_011512369.1:n.-106C>T
NM_054027.5:c.-106C>T NP_473368.1:n.-106C>T
NM_054027.6:c.-106C>T MANE Select NP_473368.1:n.-106C>T