Canonical Allele Identifier: CA155829836
Gene:

Linked Data

dbSNP Id: rs768637913
gnomAD v4: 7-24291935-G-A
MyVariant Identifiers: chr7:g.24331554G>A (hg19) chr7:g.24291935G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24291935G>A , CM000669.2:g.24291935G>A GRCh38
NC_000007.13:g.24331554G>A , CM000669.1:g.24331554G>A GRCh37
NC_000007.12:g.24298079G>A NCBI36
NG_016148.1:g.12748G>A

Transcript Alleles

HGVS Amino-acid Change
XM_017012910.1:c.41+27422C>T XP_016868399.1:n.41+27422C>T
XM_017012911.1:c.41+27422C>T XP_016868400.1:n.41+27422C>T
XR_001745121.1:n.473+27422C>T
XR_001745122.1:n.345-94906C>T
XR_001745123.1:n.473+27422C>T
XR_001745124.1:n.473+27422C>T
XR_001745125.1:n.473+27422C>T
XR_001745126.1:n.473+27422C>T
XR_001745127.1:n.345-36236C>T
XR_001745129.1:n.473+27422C>T
XR_001745130.1:n.473+27422C>T
XR_001745131.1:n.473+27422C>T
XR_001745132.1:n.473+27422C>T
Search 100 bp 5'
Search 100 bp 3'