Canonical Allele Identifier: CA1073473861
Gene: ANKH HGNC NCBI

Linked Data

gnomAD v3: 5-14871622-G-A
gnomAD v4: 5-14871622-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14871622G>A , CM000667.2:g.14871622G>A GRCh38
NC_000005.9:g.14871731G>A , CM000667.1:g.14871731G>A GRCh37
NC_000005.8:g.14924731G>A NCBI36
NG_008273.1:g.5157C>T
NG_008273.2:g.5164C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.-175C>T MANE Select ENSP00000284268.6:n.-175C>T
ENST00000284268.6:c.-175C>T ENSP00000284268.6:n.-175C>T
ENST00000505140.1:c.-175C>T ENSP00000426332.1:n.-175C>T
NM_054027.4:c.-175C>T NP_473368.1:n.-175C>T
XM_011514067.1:c.-175C>T XP_011512369.1:n.-175C>T
NM_054027.5:c.-175C>T NP_473368.1:n.-175C>T
NM_054027.6:c.-175C>T MANE Select NP_473368.1:n.-175C>T