Canonical Allele Identifier: CA2673310734

Gene: ANKH

Linked Data

• gnomAD v4: 5-14717011-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.14717011C>A , CM000667.2:g.14717011C>A	GRCh38
NC_000005.9:g.14717120C>A , CM000667.1:g.14717120C>A	GRCh37
NC_000005.8:g.14770120C>A	NCBI36
NG_008273.1:g.159768G>T
NG_008273.2:g.159775G>T
NG_051625.1:g.61218C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284268.8:c.1012-176G>T MANE Select	ENSP00000284268.6:n.1012-176G>T
ENST00000284268.6:c.1012-176G>T	ENSP00000284268.6:n.1012-176G>T
ENST00000502585.1:n.78G>T
NM_054027.4:c.1012-176G>T	NP_473368.1:n.1012-176G>T
NM_054027.5:c.1012-176G>T	NP_473368.1:n.1012-176G>T
XM_017009644.2:c.928-176G>T	XP_016865133.1:n.928-176G>T
NM_054027.6:c.1012-176G>T MANE Select	NP_473368.1:n.1012-176G>T