Canonical Allele Identifier: CA1528949089

Gene: ANKH

Linked Data

• dbSNP Id: rs1735822517

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.14871460G>C , CM000667.2:g.14871460G>C	GRCh38
NC_000005.9:g.14871569G>C , CM000667.1:g.14871569G>C	GRCh37
NC_000005.8:g.14924569G>C	NCBI36
NG_008273.1:g.5319C>G
NG_008273.2:g.5326C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284268.8:c.-13C>G MANE Select	ENSP00000284268.6:n.-13C>G
ENST00000284268.6:c.-13C>G	ENSP00000284268.6:n.-13C>G
ENST00000505140.1:c.-13C>G	ENSP00000426332.1:n.-13C>G
ENST00000513115.1:n.13C>G
NM_054027.4:c.-13C>G	NP_473368.1:n.-13C>G
XM_011514067.1:c.-13C>G	XP_011512369.1:n.-13C>G
NM_054027.5:c.-13C>G	NP_473368.1:n.-13C>G
NM_054027.6:c.-13C>G MANE Select	NP_473368.1:n.-13C>G