Canonical Allele Identifier: CA660863699
Gene:

Linked Data

dbSNP Id: rs1237319341
gnomAD v3: 10-122458302-A-G
gnomAD v4: 10-122458302-A-G
MyVariant Identifiers: chr10:g.124217818A>G (hg19) chr10:g.122458302A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122458302A>G , CM000672.2:g.122458302A>G GRCh38
NC_000010.10:g.124217818A>G , CM000672.1:g.124217818A>G GRCh37
NC_000010.9:g.124207808A>G NCBI36
NG_011554.1:g.1778A>G
NG_011725.1:g.8640A>G

Transcript Alleles

HGVS Amino-acid Change
XR_946382.1:n.1827+193T>C
XR_946383.1:n.1827+193T>C
XR_946384.1:n.1576+193T>C
XR_946385.1:n.1827+193T>C
XR_946382.2:n.1855+193T>C
XR_946383.2:n.1855+193T>C
XR_946384.2:n.1580+193T>C
XR_946385.2:n.1855+193T>C
Search 100 bp 5'
Search 100 bp 3'