Canonical Allele Identifier: CA103381336
Gene:

Linked Data

dbSNP Id: rs969287239
gnomAD v3: 4-105542955-G-C
gnomAD v4: 4-105542955-G-C
MyVariant Identifiers: chr4:g.106464112G>C (hg19) chr4:g.105542955G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542955G>C , CM000666.2:g.105542955G>C GRCh38
NC_000004.11:g.106464112G>C , CM000666.1:g.106464112G>C GRCh37
NC_000004.10:g.106683561G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.296-246C>G
XR_939039.1:n.456-246C>G
XR_939040.1:n.296-1479C>G
XR_001741410.1:n.311-246C>G
XR_001741411.1:n.787-246C>G
XR_001741412.1:n.311-246C>G
XR_001741413.1:n.311-246C>G
XR_001741414.1:n.311-246C>G
XR_939038.2:n.311-246C>G
XR_939040.2:n.311-1479C>G
Search 100 bp 5'
Search 100 bp 3'