Canonical Allele Identifier: CA103381335
Gene:

Linked Data

dbSNP Id: rs536550427
MyVariant Identifiers: chr4:g.106464108C>G (hg19) chr4:g.105542951C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542951C>G , CM000666.2:g.105542951C>G GRCh38
NC_000004.11:g.106464108C>G , CM000666.1:g.106464108C>G GRCh37
NC_000004.10:g.106683557C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.296-242G>C
XR_939039.1:n.456-242G>C
XR_939040.1:n.296-1475G>C
XR_001741410.1:n.311-242G>C
XR_001741411.1:n.787-242G>C
XR_001741412.1:n.311-242G>C
XR_001741413.1:n.311-242G>C
XR_001741414.1:n.311-242G>C
XR_939038.2:n.311-242G>C
XR_939040.2:n.311-1475G>C
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