Canonical Allele Identifier: CA3209246
Gene: ANKH HGNC NCBI

Linked Data

dbSNP Id: rs544582199
gnomAD v2: 5-14871446-G-C
gnomAD v3: 5-14871337-G-C
gnomAD v4: 5-14871337-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14871337G>C , CM000667.2:g.14871337G>C GRCh38
NC_000005.9:g.14871446G>C , CM000667.1:g.14871446G>C GRCh37
NC_000005.8:g.14924446G>C NCBI36
NG_008273.1:g.5442C>G
NG_008273.2:g.5449C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.96+15C>G MANE Select ENSP00000284268.6:n.96+15C>G
ENST00000284268.6:c.96+15C>G ENSP00000284268.6:n.96+15C>G
ENST00000505140.1:c.111C>G ENSP00000426332.1:p.Pro37=
ENST00000513115.1:n.121+15C>G
NM_054027.4:c.96+15C>G NP_473368.1:n.96+15C>G
XM_011514067.1:c.96+15C>G XP_011512369.1:n.96+15C>G
NM_054027.5:c.96+15C>G NP_473368.1:n.96+15C>G
NM_054027.6:c.96+15C>G MANE Select NP_473368.1:n.96+15C>G