Canonical Allele Identifier: CA305499690
Gene: KLF1 HGNC NCBI

Linked Data

dbSNP Id: rs1049883835
MyVariant Identifiers: chr19:g.12997912T>C (hg19) chr19:g.12887098T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12887098T>C , CM000681.2:g.12887098T>C GRCh38
NC_000019.9:g.12997912T>C , CM000681.1:g.12997912T>C GRCh37
NC_000019.8:g.12858912T>C NCBI36
NG_009292.1:g.939T>C
NG_013087.1:g.5106A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264834.6:c.43A>G MANE Select ENSP00000264834.3:p.Thr15Ala
ENST00000264834.4:c.43A>G ENSP00000264834.3:p.Thr15Ala
NM_006563.3:c.43A>G NP_006554.1:p.Thr15Ala
XM_011527642.1:c.-161A>G XP_011525944.1:n.-161A>G
NM_006563.4:c.43A>G NP_006554.1:p.Thr15Ala
XM_011527642.2:c.-161A>G XP_011525944.1:n.-161A>G
NM_006563.5:c.43A>G MANE Select NP_006554.1:p.Thr15Ala
Search 100 bp 5'
Search 100 bp 3'