Canonical Allele Identifier: CA936776395

Gene:

Linked Data

• dbSNP Id: rs1696614288
• gnomAD v3: 11-34759462-G-T
• gnomAD v4: 11-34759462-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.34759462G>T , CM000673.2:g.34759462G>T	GRCh38
NC_000011.9:g.34781009G>T , CM000673.1:g.34781009G>T	GRCh37
NC_000011.8:g.34737585G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_428897.2:n.579+4855G>T
XR_931188.1:n.693+4855G>T
XR_931189.1:n.854+4855G>T
XR_931190.1:n.639+4855G>T
XR_931191.1:n.689+4855G>T
XR_001748174.1:n.855+4855G>T
XR_001748176.1:n.1016+4855G>T
XR_002957246.1:n.639+4855G>T