Canonical Allele Identifier: CA1482797501
Gene:

Linked Data

dbSNP Id: rs1724779618

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542518T>C , CM000666.2:g.105542518T>C GRCh38
NC_000004.11:g.106463675T>C , CM000666.1:g.106463675T>C GRCh37
NC_000004.10:g.106683124T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939038.1:n.487A>G
XR_939039.1:n.647A>G
XR_939040.1:n.296-1042A>G
XR_001741410.1:n.502A>G
XR_001741411.1:n.978A>G
XR_001741412.1:n.449+53A>G
XR_001741413.1:n.502A>G
XR_001741414.1:n.449+53A>G
XR_939038.2:n.502A>G
XR_939040.2:n.311-1042A>G