Canonical Allele Identifier: CA754920640

Gene: EDAR RANBP2

Linked Data

• dbSNP Id: rs1189514537
• gnomAD v3: 2-108958988-T-A
• gnomAD v4: 2-108958988-T-A
• MyVariant Identifiers: chr2:g.109575444T>A (hg19) ; chr2:g.108958988T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108958988T>A , CM000664.2:g.108958988T>A	GRCh38
NC_000002.11:g.109575444T>A , CM000664.1:g.109575444T>A	GRCh37
NC_000002.10:g.108941876T>A	NCBI36
NG_008257.1:g.35385A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258443.7:c.-18-27956A>T (EDAR) MANE Select	ENSP00000258443.2:n.-18-27956A>T
ENST00000258443.6:c.-18-27956A>T (EDAR)	ENSP00000258443.2:n.-18-27956A>T
ENST00000376651.1:c.-18-27956A>T (EDAR)	ENSP00000365839.1:n.-18-27956A>T
ENST00000409271.5:c.-134-18662A>T (EDAR)	ENSP00000386371.1:n.-134-18662A>T
NM_022336.3:c.-18-27956A>T (EDAR)	NP_071731.1:n.-18-27956A>T
XM_006712204.1:c.-18-27956A>T (EDAR)	XP_006712267.1:n.-18-27956A>T
XM_011510502.1:c.33+6635A>T (EDAR)	XP_011508804.1:n.33+6635A>T
XM_011510503.1:c.33+6635A>T (EDAR)	XP_011508805.1:n.33+6635A>T
XM_011510502.2:c.126+6635A>T (EDAR)	XP_011508804.2:n.126+6635A>T
XM_011510503.2:c.126+6635A>T (EDAR)	XP_011508805.2:n.126+6635A>T
XM_017004623.2:c.8370+185942T>A (RANBP2)	XP_016860112.1:n.8370+185942T>A
NM_022336.4:c.-18-27956A>T (EDAR) MANE Select	NP_071731.1:n.-18-27956A>T