Canonical Allele Identifier: CA359253852
Gene: ANKH HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.14769263G>C (hg19) chr5:g.14769154G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14769154G>C , CM000667.2:g.14769154G>C GRCh38
NC_000005.9:g.14769263G>C , CM000667.1:g.14769263G>C GRCh37
NC_000005.8:g.14822263G>C NCBI36
NG_008273.1:g.107625C>G
NG_008273.2:g.107632C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.134C>G MANE Select ENSP00000284268.6:p.Ala45Gly
ENST00000284268.6:c.134C>G ENSP00000284268.6:p.Ala45Gly
ENST00000503389.1:n.140C>G
ENST00000513115.1:n.159C>G
NM_054027.4:c.134C>G NP_473368.1:p.Ala45Gly
XM_011514067.1:c.134C>G XP_011512369.1:p.Ala45Gly
NM_054027.5:c.134C>G NP_473368.1:p.Ala45Gly
XM_017009644.2:c.50C>G XP_016865133.1:p.Ala17Gly
NM_054027.6:c.134C>G MANE Select NP_473368.1:p.Ala45Gly
Search 100 bp 5'
Search 100 bp 3'