Canonical Allele Identifier: CA14378849
Gene: STAT5B HGNC NCBI

Linked Data

dbSNP Id: rs4029774

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42276943A>G , CM000679.2:g.42276943A>G GRCh38
NC_000017.10:g.40428961A>G , CM000679.1:g.40428961A>G GRCh37
NC_000017.9:g.37682487A>G NCBI36
NG_007271.1:g.4464T>C , LRG_192:g.4464T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000698776.1:c.-11+10844T>C ENSP00000513923.1:n.-11+10844T>C
ENST00000698777.1:c.-11+11517T>C ENSP00000513924.1:n.-11+11517T>C
XM_024450897.1:c.-11+10844T>C XP_024306665.1:n.-11+10844T>C