Canonical Allele Identifier: CA440675772
Gene:

Linked Data

MyVariant Identifiers: chr4:g.106463730T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542573T>C , CM000666.2:g.105542573T>C GRCh38
NC_000004.11:g.106463730T>C , CM000666.1:g.106463730T>C GRCh37
NC_000004.10:g.106683179T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939038.1:n.432A>G
XR_939039.1:n.592A>G
XR_939040.1:n.296-1097A>G
XR_001741410.1:n.447A>G
XR_001741411.1:n.923A>G
XR_001741412.1:n.447A>G
XR_001741413.1:n.447A>G
XR_001741414.1:n.447A>G
XR_939038.2:n.447A>G
XR_939040.2:n.311-1097A>G