Canonical Allele Identifier: CA2578273264
Gene: ANKH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14716930A>G , CM000667.2:g.14716930A>G GRCh38
NC_000005.9:g.14717039A>G , CM000667.1:g.14717039A>G GRCh37
NC_000005.8:g.14770039A>G NCBI36
NG_008273.1:g.159849T>C
NG_008273.2:g.159856T>C
NG_051625.1:g.61137A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.1012-95T>C MANE Select ENSP00000284268.6:n.1012-95T>C
ENST00000284268.6:c.1012-95T>C ENSP00000284268.6:n.1012-95T>C
ENST00000502585.1:n.159T>C
NM_054027.4:c.1012-95T>C NP_473368.1:n.1012-95T>C
NM_054027.5:c.1012-95T>C NP_473368.1:n.1012-95T>C
XM_017009644.2:c.928-95T>C XP_016865133.1:n.928-95T>C
NM_054027.6:c.1012-95T>C MANE Select NP_473368.1:n.1012-95T>C