Canonical Allele Identifier: CA2670966276

Gene: ALB

Linked Data

• gnomAD v4: 4-73418081-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418081T>C , CM000666.2:g.73418081T>C	GRCh38
NC_000004.11:g.74283798T>C , CM000666.1:g.74283798T>C	GRCh37
NC_000004.10:g.74502662T>C	NCBI36
NG_009291.1:g.18827T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1429-7T>C MANE Select	ENSP00000295897.4:n.1429-7T>C
ENST00000295897.8:c.1429-7T>C	ENSP00000295897.4:n.1429-7T>C
ENST00000401494.7:c.1084-7T>C	ENSP00000384695.3:n.1084-7T>C
ENST00000415165.6:c.853-7T>C	ENSP00000401820.2:n.853-7T>C
ENST00000476441.6:c.*708-7T>C	ENSP00000423727.1:n.*708-7T>C
ENST00000486939.1:n.76T>C
ENST00000503124.5:c.979-7T>C	ENSP00000421027.1:n.979-7T>C
ENST00000505649.5:n.976-7T>C
ENST00000509063.5:c.1429-7T>C	ENSP00000422784.1:n.1429-7T>C
ENST00000511370.1:c.962-7T>C
ENST00000621085.4:c.790-7T>C	ENSP00000483421.1:n.790-7T>C
ENST00000621628.4:c.790-7T>C	ENSP00000480485.1:n.790-7T>C
NM_000477.5:c.1429-7T>C	NP_000468.1:n.1429-7T>C
NM_000477.6:c.1429-7T>C	NP_000468.1:n.1429-7T>C
NM_000477.7:c.1429-7T>C MANE Select	NP_000468.1:n.1429-7T>C