Canonical Allele Identifier: CA2670937054

Gene: ALB

Linked Data

• gnomAD v4: 4-73408934-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73408934T>C , CM000666.2:g.73408934T>C	GRCh38
NC_000004.11:g.74274651T>C , CM000666.1:g.74274651T>C	GRCh37
NC_000004.10:g.74493515T>C	NCBI36
NG_009291.1:g.9680T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.482+129T>C MANE Select	ENSP00000295897.4:n.482+129T>C
ENST00000295897.8:c.482+129T>C	ENSP00000295897.4:n.482+129T>C
ENST00000401494.7:c.138-421T>C	ENSP00000384695.3:n.138-421T>C
ENST00000415165.6:c.138-3062T>C	ENSP00000401820.2:n.138-3062T>C
ENST00000441319.5:c.488+129T>C	ENSP00000392541.1:n.488+129T>C
ENST00000476441.6:c.80-421T>C	ENSP00000423727.1:n.80-421T>C
ENST00000503124.5:c.33-421T>C	ENSP00000421027.1:n.33-421T>C
ENST00000505649.5:n.168+129T>C
ENST00000509063.5:c.482+129T>C	ENSP00000422784.1:n.482+129T>C
ENST00000514786.1:n.451+129T>C
ENST00000515133.5:n.652T>C
ENST00000621085.4:c.482+129T>C	ENSP00000483421.1:n.482+129T>C
ENST00000621628.4:c.482+129T>C	ENSP00000480485.1:n.482+129T>C
NM_000477.5:c.482+129T>C	NP_000468.1:n.482+129T>C
NM_000477.6:c.482+129T>C	NP_000468.1:n.482+129T>C
NM_000477.7:c.482+129T>C MANE Select	NP_000468.1:n.482+129T>C