Canonical Allele Identifier: CA2673310638
Gene: ANKH HGNC NCBI

Linked Data

gnomAD v4: 5-14716956-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14716956G>T , CM000667.2:g.14716956G>T GRCh38
NC_000005.9:g.14717065G>T , CM000667.1:g.14717065G>T GRCh37
NC_000005.8:g.14770065G>T NCBI36
NG_008273.1:g.159823C>A
NG_008273.2:g.159830C>A
NG_051625.1:g.61163G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.1012-121C>A MANE Select ENSP00000284268.6:n.1012-121C>A
ENST00000284268.6:c.1012-121C>A ENSP00000284268.6:n.1012-121C>A
ENST00000502585.1:n.133C>A
NM_054027.4:c.1012-121C>A NP_473368.1:n.1012-121C>A
NM_054027.5:c.1012-121C>A NP_473368.1:n.1012-121C>A
XM_017009644.2:c.928-121C>A XP_016865133.1:n.928-121C>A
NM_054027.6:c.1012-121C>A MANE Select NP_473368.1:n.1012-121C>A
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