Canonical Allele Identifier: CA1073473799
Gene: ANKH HGNC NCBI

Linked Data

dbSNP Id: rs1735829536
gnomAD v3: 5-14871556-G-A
gnomAD v4: 5-14871556-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14871556G>A , CM000667.2:g.14871556G>A GRCh38
NC_000005.9:g.14871665G>A , CM000667.1:g.14871665G>A GRCh37
NC_000005.8:g.14924665G>A NCBI36
NG_008273.1:g.5223C>T
NG_008273.2:g.5230C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.-109C>T MANE Select ENSP00000284268.6:n.-109C>T
ENST00000284268.6:c.-109C>T ENSP00000284268.6:n.-109C>T
ENST00000505140.1:c.-109C>T ENSP00000426332.1:n.-109C>T
NM_054027.4:c.-109C>T NP_473368.1:n.-109C>T
XM_011514067.1:c.-109C>T XP_011512369.1:n.-109C>T
NM_054027.5:c.-109C>T NP_473368.1:n.-109C>T
NM_054027.6:c.-109C>T MANE Select NP_473368.1:n.-109C>T