Canonical Allele Identifier: CA3208925
Gene: ANKH HGNC NCBI

Linked Data

dbSNP Id: rs758021005
gnomAD v2: 5-14716876-G-A
gnomAD v3: 5-14716767-G-A
gnomAD v4: 5-14716767-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14716767G>A , CM000667.2:g.14716767G>A GRCh38
NC_000005.9:g.14716876G>A , CM000667.1:g.14716876G>A GRCh37
NC_000005.8:g.14769876G>A NCBI36
NG_008273.1:g.160012C>T
NG_008273.2:g.160019C>T
NG_051625.1:g.60974G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.1080C>T MANE Select ENSP00000284268.6:p.Asp360=
ENST00000284268.6:c.1080C>T ENSP00000284268.6:p.Asp360=
ENST00000502585.1:n.322C>T
NM_054027.4:c.1080C>T NP_473368.1:p.Asp360=
NM_054027.5:c.1080C>T NP_473368.1:p.Asp360=
XM_017009644.2:c.996C>T XP_016865133.1:p.Asp332=
NM_054027.6:c.1080C>T MANE Select NP_473368.1:p.Asp360=