Canonical Allele Identifier: CA2673314799
Gene: ANKH HGNC NCBI

Linked Data

gnomAD v4: 5-14871554-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14871554A>C , CM000667.2:g.14871554A>C GRCh38
NC_000005.9:g.14871663A>C , CM000667.1:g.14871663A>C GRCh37
NC_000005.8:g.14924663A>C NCBI36
NG_008273.1:g.5225T>G
NG_008273.2:g.5232T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.-107T>G MANE Select ENSP00000284268.6:n.-107T>G
ENST00000284268.6:c.-107T>G ENSP00000284268.6:n.-107T>G
ENST00000505140.1:c.-107T>G ENSP00000426332.1:n.-107T>G
NM_054027.4:c.-107T>G NP_473368.1:n.-107T>G
XM_011514067.1:c.-107T>G XP_011512369.1:n.-107T>G
NM_054027.5:c.-107T>G NP_473368.1:n.-107T>G
NM_054027.6:c.-107T>G MANE Select NP_473368.1:n.-107T>G
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