Canonical Allele Identifier: CA557887463
Gene: ANKH HGNC NCBI

Linked Data

dbSNP Id: rs746523638
gnomAD v2: 5-14716766-T-G
gnomAD v3: 5-14716657-T-G
gnomAD v4: 5-14716657-T-G
MyVariant Identifiers: chr5:g.14716766T>G (hg19) chr5:g.14716657T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14716657T>G , CM000667.2:g.14716657T>G GRCh38
NC_000005.9:g.14716766T>G , CM000667.1:g.14716766T>G GRCh37
NC_000005.8:g.14769766T>G NCBI36
NG_008273.1:g.160122A>C
NG_008273.2:g.160129A>C
NG_051625.1:g.60864T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.1141+49A>C MANE Select ENSP00000284268.6:n.1141+49A>C
ENST00000284268.6:c.1141+49A>C ENSP00000284268.6:n.1141+49A>C
ENST00000502585.1:n.383+49A>C
NM_054027.4:c.1141+49A>C NP_473368.1:n.1141+49A>C
NM_054027.5:c.1141+49A>C NP_473368.1:n.1141+49A>C
XM_017009644.2:c.1057+49A>C XP_016865133.1:n.1057+49A>C
NM_054027.6:c.1141+49A>C MANE Select NP_473368.1:n.1141+49A>C
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