Canonical Allele Identifier: CA2734141304
Gene: NHERF1 HGNC NCBI

Linked Data

dbSNP Id: rs2144122674
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.74763336T>C , CM000679.2:g.74763336T>C GRCh38
NC_000017.10:g.72759475T>C , CM000679.1:g.72759475T>C GRCh37
NC_000017.9:g.70271070T>C NCBI36
NG_013022.1:g.19713T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000262613.10:c.604-31T>C MANE Select ENSP00000262613.5:n.604-31T>C
ENST00000262613.9:c.604-31T>C ENSP00000262613.5:n.604-31T>C
ENST00000413388.2:c.136-31T>C ENSP00000464982.1:n.136-31T>C
ENST00000578958.1:n.307T>C
ENST00000583369.5:c.442-4811T>C ENSP00000464321.1:n.442-4811T>C
NM_004252.4:c.604-31T>C NP_004243.1:n.604-31T>C
XR_002958087.1:n.823-31T>C
NM_004252.5:c.604-31T>C MANE Select NP_004243.1:n.604-31T>C
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