Canonical Allele Identifier: CA114719997
Gene: ANKH HGNC NCBI

Linked Data

dbSNP Id: rs914529221
gnomAD v3: 5-14716635-C-T
gnomAD v4: 5-14716635-C-T
MyVariant Identifiers: chr5:g.14716744C>T (hg19) chr5:g.14716635C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14716635C>T , CM000667.2:g.14716635C>T GRCh38
NC_000005.9:g.14716744C>T , CM000667.1:g.14716744C>T GRCh37
NC_000005.8:g.14769744C>T NCBI36
NG_008273.1:g.160144G>A
NG_008273.2:g.160151G>A
NG_051625.1:g.60842C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000284268.8:c.1141+71G>A MANE Select ENSP00000284268.6:n.1141+71G>A
ENST00000284268.6:c.1141+71G>A ENSP00000284268.6:n.1141+71G>A
ENST00000502585.1:n.383+71G>A
NM_054027.4:c.1141+71G>A NP_473368.1:n.1141+71G>A
NM_054027.5:c.1141+71G>A NP_473368.1:n.1141+71G>A
XM_017009644.2:c.1057+71G>A XP_016865133.1:n.1057+71G>A
NM_054027.6:c.1141+71G>A MANE Select NP_473368.1:n.1141+71G>A
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