Canonical Allele Identifier: CA726314738
Gene: YWHAE HGNC NCBI

Linked Data

dbSNP Id: rs1363783654
gnomAD v3: 17-1400354-C-T
gnomAD v4: 17-1400354-C-T
MyVariant Identifiers: chr17:g.1303648C>T (hg19) chr17:g.1400354C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1400354C>T , CM000679.2:g.1400354C>T GRCh38
NC_000017.10:g.1303648C>T , CM000679.1:g.1303648C>T GRCh37
NC_000017.9:g.1250398C>T NCBI36
NG_009233.1:g.4909G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264335.12:c.-244G>A ENSP00000264335.8:n.-244G>A
XM_005256784.2:c.-244G>A XP_005256841.1:n.-244G>A
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